A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025280



Internal ID18767812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121615257..121736740hg38UCSC Ensembl
Innerchr6:121936403..122057886hg19UCSC Ensembl
Innerchr6:121978102..122099585hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38121484
hg19121484
hg18121484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654342
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)nsv1025280
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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