A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111776



Internal ID18908558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495842..76501242hg38UCSC Ensembl
Outerchr10:78255600..78261000hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv480n106
Supporting Variantsnssv3960418, nssv3988869
SamplesKWS2, KWS1
Known GenesC10orf11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111776
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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