A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043320



Internal ID19132539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126166640..126192278hg38UCSC Ensembl
Innerchr9:128928919..128954557hg19UCSC Ensembl
Innerchr9:127968740..127994378hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3825639
hg1925639
hg1825639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695240
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043320
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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