A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746855



Internal ID15694125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38022849..38212726hg38UCSC Ensembl
Innerchr10:38311777..38501654hg19UCSC Ensembl
Innerchr10:38351783..38541660hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38189878
hg19189878
hg18189878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550419
Supporting Variants
Samples
Known GenesLOC100129055, ZNF33A, ZNF37A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746855
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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