A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503999



Internal ID18802280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55679434..55971344hg38UCSC Ensembl
Innerchr10:57439194..57731104hg19UCSC Ensembl
Innerchr10:57109200..57401110hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38291911
hg19291911
hg18291911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035651
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)nssv3503999
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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