A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022760



Internal ID19111978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66238608..66726214hg38UCSC Ensembl
Innerchr6:66948501..67436107hg19UCSC Ensembl
Innerchr6:67005222..67492828hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38487607
hg19487607
hg18487607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745574, nssv3745573
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)nsv1022760
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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