A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029022



Internal ID18771554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88521483..89890325hg38UCSC Ensembl
Innerchr7:88150798..89519639hg19UCSC Ensembl
Innerchr7:87988734..89357575hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381368843
hg191368842
hg181368842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6526n100
Supporting Variantsnssv3655201
Samples
Known GenesC7orf62, ZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029022
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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