A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044176



Internal ID19133395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80862128..80877955hg38UCSC Ensembl
Innerchr9:83477043..83492870hg19UCSC Ensembl
Innerchr9:82666863..82682690hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3815828
hg1915828
hg1815828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697518
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)nsv1044176
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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