A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020892



Internal ID19110110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55536706..55569330hg38UCSC Ensembl
Innerchr7:55604399..55637023hg19UCSC Ensembl
Innerchr7:55571893..55604517hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3832625
hg1932625
hg1832625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6361n100
Supporting Variantsnssv3661415
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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