A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020427



Internal ID19109646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52854943..52921859hg38UCSC Ensembl
Innerchr7:52922636..52989552hg19UCSC Ensembl
Innerchr7:52890130..52957046hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3866917
hg1966917
hg1866917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6349n100
Supporting Variantsnssv3661279
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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