A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716733



Internal ID19015014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55210310..55263496hg38UCSC Ensembl
Innerchr15:55502508..55555694hg19UCSC Ensembl
Innerchr15:53289800..53342986hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3853187
hg1953187
hg1853187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049977
Supporting Variants
Samples
Known GenesRAB27A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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