A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568743



Internal ID16009466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30349223..30475410hg38UCSC Ensembl
Innerchr15:30641426..30767613hg19UCSC Ensembl
Innerchr15:28428718..28554905hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38126188
hg19126188
hg18126188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4422n54
Supporting Variantsnssv839472, nssv839471
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568743
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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