A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134122



Internal ID15987308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67384759..67420766hg38UCSC Ensembl
Innerchr9:40123292..40159571hg19UCSC Ensembl
Innerchr9:40113292..40149571hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3836008
hg1936280
hg1836280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614305
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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