A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021867



Internal ID19111085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65105195..65626699hg38UCSC Ensembl
Innerchr7:64565573..65091612hg19UCSC Ensembl
Innerchr7:64203008..64729047hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38521505
hg19526040
hg18526040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3655509
Samples
Known GenesZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021867
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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