A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156443



Internal ID15533377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3349487..3389660hg38UCSC Ensembl
Innerchr9:3349487..3389660hg19UCSC Ensembl
Innerchr9:3339487..3379660hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3840174
hg1940174
hg1840174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613146
Supporting Variants
SamplesNINDS_147
Known GenesRFX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156443
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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