A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503012



Internal ID18801293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121669087..121692680hg38UCSC Ensembl
Innerchr10:123428601..123452194hg19UCSC Ensembl
Innerchr10:123418591..123442184hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823594
hg1923594
hg1823594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036499
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3503012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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