A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016344



Internal ID19105563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19535054..19615001hg38UCSC Ensembl
Innerchr7:19574677..19654624hg19UCSC Ensembl
Innerchr7:19541202..19621149hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3879948
hg1979948
hg1879948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6304n100
Supporting Variantsnssv3643259
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)nsv1016344
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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