A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148251



Internal ID16001437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135705128..135761806hg38UCSC Ensembl
Innerchr9:138596974..138653652hg19UCSC Ensembl
Innerchr9:137736795..137793473hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3856679
hg1956679
hg1856679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615924
Supporting Variants
Samples
Known GenesKCNT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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