A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716728



Internal ID19015009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53062088..53106482hg38UCSC Ensembl
Innerchr15:53354285..53398679hg19UCSC Ensembl
Innerchr15:51141577..51185971hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3844395
hg1944395
hg1844395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036751
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)nssv3716728
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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