A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035631



Internal ID19124850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104877181..105243289hg38UCSC Ensembl
Innerchr13:105529532..105895640hg19UCSC Ensembl
Innerchr13:104327533..104693641hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38366109
hg19366109
hg18366109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1738n100
Supporting Variantsnssv3525554
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)nsv1035631
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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