A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777159



Internal ID15724429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64566642..64759608hg38UCSC Ensembl
Innerchr11:64334114..64527080hg19UCSC Ensembl
Innerchr11:64090690..64283656hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38192967
hg19192967
hg18192967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555195
Supporting Variants
Samples
Known GenesNRXN2, PYGM, RASGRP2, SLC22A11, SLC22A12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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