A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022625



Internal ID19111843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:8592266..8718879hg38UCSC Ensembl
Innerchr6:8592499..8719112hg19UCSC Ensembl
Innerchr6:8537498..8664111hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38126614
hg19126614
hg18126614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5915n100
Supporting Variantsnssv3654752, nssv3654753, nssv3749019
Samples
Known GenesHULC, LOC100506207
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022625
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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