A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015520



Internal ID19104737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80599496..80664982hg38UCSC Ensembl
Innerchr6:81309213..81374699hg19UCSC Ensembl
Innerchr6:81365932..81431418hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3865487
hg1965487
hg1865487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648859
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)nsv1015520
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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