A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022595



Internal ID19111813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42697890..42834341hg38UCSC Ensembl
Innerchr9:44136778..44273229hg19UCSC Ensembl
Innerchr9:44076774..44213225hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38136452
hg19136452
hg18136452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3693046, nssv3756868
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)nsv1022595
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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