A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555255



Internal ID18853536
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 StatusS
Merged Variantsnsv1036696
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)nssv3555255
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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