A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037530



Internal ID19126749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27672432..27687762hg38UCSC Ensembl
Innerchr15:27917578..27932908hg19UCSC Ensembl
Innerchr15:25591173..25606503hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3815331
hg1915331
hg1815331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2488n100
Supporting Variantsnssv3545651, nssv3545653, nssv3545652, nssv3545650, nssv3545649
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)nsv1037530
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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