A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149270



Internal ID15507092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101300541..101324391hg38UCSC Ensembl
Innerchr15:101840746..101864596hg19UCSC Ensembl
Innerchr15:99658269..99682119hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3823851
hg1923851
hg1823851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570849
Supporting Variants
Samples1780854437_A
Known GenesLOC100507472, PCSK6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149270
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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