A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042615



Internal ID19131834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95095609..95109337hg38UCSC Ensembl
Innerchr10:96855366..96869094hg19UCSC Ensembl
Innerchr10:96845356..96859084hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3813729
hg1913729
hg1813729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv959n100
Supporting Variantsnssv3512382
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)nsv1042615
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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