A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716699



Internal ID19014980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36175444..36214754hg38UCSC Ensembl
Innerchr15:36467645..36506955hg19UCSC Ensembl
Innerchr15:34254937..34294247hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3839311
hg1939311
hg1839311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042905
Supporting Variants
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)nssv3716699
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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