A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027639



Internal ID19116858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64075823..64330891hg38UCSC Ensembl
Innerchr7:63536201..63791269hg19UCSC Ensembl
Innerchr7:63173636..63428704hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38255069
hg19255069
hg18255069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6434n100
Supporting Variantsnssv3661974
Samples
Known GenesZNF679, ZNF727, ZNF735, ZNF736
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027639
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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