A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016391



Internal ID19105610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42324206..42353109hg38UCSC Ensembl
Innerchr7:42363805..42392708hg19UCSC Ensembl
Innerchr7:42330330..42359233hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3828904
hg1928904
hg1828904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6340n100
Supporting Variantsnssv3661223, nssv3661222, nssv3661221, nssv3661224
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)nsv1016391
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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