A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020964



Internal ID19110182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82015451..82027739hg38UCSC Ensembl
Innerchr6:82725168..82737456hg19UCSC Ensembl
Innerchr6:82781887..82794175hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3812289
hg1912289
hg1812289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6077n100
Supporting Variantsnssv3648881, nssv3648882
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)nsv1020964
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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