A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017971



Internal ID19107188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..6928985hg38UCSC Ensembl
Innerchr7:6854098..6968616hg19UCSC Ensembl
Innerchr7:6820623..6935141hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38114519
hg19114519
hg18114519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655077
Samples
Known GenesCCZ1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017971
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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