A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2724073



Internal ID9958374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:226975915..226976583hg38UCSC Ensembl
Outerchr1:227163616..227164284hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6675384, essv6895986, essv6847307, essv6692962, essv6777106, essv6933490, essv6968120, essv6720198, essv6773618, essv6955027, essv6859410, essv6886122, essv6729795, essv6961830, essv6937853, essv6738986, essv6753651, essv6769704, essv6810471, essv6759200, essv6785173, essv6781060, essv6836354, essv6898759, essv6832748, essv6789340, essv6697122, essv6917620, essv6840133
SamplesSSM100, SSM083, SSM027, SSM065, SSM038, SSM088, SSM058, SSM028, SSM084, SSM021, SSM047, SSM069, SSM061, SSM096, SSM026, SSM017, SSM032, SSM067, SSM086, SSM066, SSM068, SSM082, SSM007, SSM037, SSM076, SSM022, SSM070, SSM099, SSM052
Known GenesADCK3
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2724073
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer