A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141196



Internal ID15994382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110713825..110717800hg38UCSC Ensembl
Innerchr9:113476105..113480080hg19UCSC Ensembl
Innerchr9:112515926..112519901hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg383976
hg193976
hg183976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615174
Supporting Variants
Samples
Known GenesMUSK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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