A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027321



Internal ID19116540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7239198..7270363hg38UCSC Ensembl
Innerchr9:7239198..7270363hg19UCSC Ensembl
Innerchr9:7229198..7260363hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3831166
hg1931166
hg1831166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758112
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)nsv1027321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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