A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021870



Internal ID19111088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82402521..82494985hg38UCSC Ensembl
Innerchr6:83112238..83204702hg19UCSC Ensembl
Innerchr6:83168957..83261421hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3892465
hg1992465
hg1892465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648883
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)nsv1021870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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