A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6773844



Internal ID10179942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:179557205..179557818hg38UCSC Ensembl
Outerchr2:180421932..180422545hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721199
Supporting Variants
SamplesSSM066
Known GenesZNF385B
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)essv6773844
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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