A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032503



Internal ID19121725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19052837..19095372hg38UCSC Ensembl
Innerchr7:19092460..19134995hg19UCSC Ensembl
Innerchr7:19058985..19101520hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3842536
hg1942536
hg1842536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6299n100
Supporting Variantsnssv3643236, nssv3643237, nssv3643238
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)nsv1032503
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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