A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570258



Internal ID16357667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83538798..83567178hg38UCSC Ensembl
Innerchr15:84207550..84235930hg19UCSC Ensembl
Innerchr15:81998554..82026934hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3828381
hg1928381
hg1828381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149249
Samples1787431166_A
Known GenesSH3GL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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