A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545654



Internal ID18843935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27672432..27689357hg38UCSC Ensembl
Innerchr15:27917578..27934503hg19UCSC Ensembl
Innerchr15:25591173..25608098hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816926
hg1916926
hg1816926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048311
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)nssv3545654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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