A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043001



Internal ID19132220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115491602..115571621hg38UCSC Ensembl
Innerchr9:118253881..118333900hg19UCSC Ensembl
Innerchr9:117293702..117373721hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3880020
hg1980020
hg1880020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695161
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)nsv1043001
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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