A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031360



Internal ID19120582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112715806..112980035hg38UCSC Ensembl
Innerchr6:113037008..113301237hg19UCSC Ensembl
Innerchr6:113143701..113407930hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38264230
hg19264230
hg18264230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654302
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)nsv1031360
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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