A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570171



Internal ID16357580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77772322..77838755hg38UCSC Ensembl
Innerchr15:78064664..78131097hg19UCSC Ensembl
Innerchr15:75851719..75918152hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3866434
hg1966434
hg1866434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149242
SamplesHGDP00830
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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