A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031269



Internal ID18773802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17204322..17316971hg38UCSC Ensembl
Innerchr9:17204320..17316969hg19UCSC Ensembl
Innerchr9:17194320..17306969hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38112650
hg19112650
hg18112650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690646
Samples
Known GenesCNTLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031269
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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