A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017572



Internal ID19106789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14830279..14906702hg38UCSC Ensembl
Innerchr6:14830510..14906933hg19UCSC Ensembl
Innerchr6:14938489..15014912hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3876424
hg1976424
hg1876424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654793
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)nsv1017572
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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