A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815776



Internal ID16109732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635745..75636921hg38UCSC Ensembl
Innerchr13:76209881..76211057hg19UCSC Ensembl
Innerchr13:75107882..75109058hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381177
hg191177
hg181177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562355
Supporting Variants
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv815776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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