A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046386



Internal ID19135605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109445261..109574018hg38UCSC Ensembl
Innerchr10:111205019..111333776hg19UCSC Ensembl
Innerchr10:111195009..111323766hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38128758
hg19128758
hg18128758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502993, nssv3706236, nssv3504716, nssv3706235, nssv3502802, nssv3520388
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)nsv1046386
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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