A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032958



Internal ID19122180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19922565..19959249hg38UCSC Ensembl
Innerchr9:19922563..19959247hg19UCSC Ensembl
Innerchr9:19912563..19949247hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3836685
hg1936685
hg1836685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690692
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)nsv1032958
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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