A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018590



Internal ID19107807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65133951..65615363hg38UCSC Ensembl
Innerchr7:64594329..65080276hg19UCSC Ensembl
Innerchr7:64231764..64717711hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38481413
hg19485948
hg18485948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6435n100
Supporting Variantsnssv3655522
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)nsv1018590
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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