A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036696



Internal ID19125915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93598378..93625983hg38UCSC Ensembl
Innerchr15:94141607..94169212hg19UCSC Ensembl
Innerchr15:91942611..91970216hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3827606
hg1927606
hg1827606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2663n100
Supporting Variantsnssv3555255
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)nsv1036696
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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