A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023478



Internal ID19112695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..6961964hg38UCSC Ensembl
Innerchr7:6854098..7001595hg19UCSC Ensembl
Innerchr7:6820623..6968120hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38147498
hg19147498
hg18147498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655078
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)nsv1023478
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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