A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570151



Internal ID16357560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77716501..77718762hg38UCSC Ensembl
Innerchr15:78008843..78011104hg19UCSC Ensembl
Innerchr15:75795898..75798159hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382262
hg192262
hg182262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4663n54
Supporting Variantsnssv847274, nssv847271, nssv847272, nssv847273, nssv847275
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570151
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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