A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707668



Internal ID19005949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4251879..4269393hg38UCSC Ensembl
Innerchr10:4294071..4311585hg19UCSC Ensembl
Innerchr10:4284071..4301585hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3817515
hg1917515
hg1817515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037897
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)nssv3707668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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