A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018962



Internal ID19108179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45028977..45070301hg38UCSC Ensembl
Innerchr6:44996714..45038038hg19UCSC Ensembl
Innerchr6:45104692..45146016hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3841325
hg1941325
hg1841325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5958n100
Supporting Variantsnssv3657435
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018962
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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