A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016655



Internal ID19105872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124935630..125044225hg38UCSC Ensembl
Innerchr7:124575684..124684279hg19UCSC Ensembl
Innerchr7:124362920..124471515hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38108596
hg19108596
hg18108596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662140
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)nsv1016655
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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