A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020530



Internal ID18763065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1870197..2658587hg38UCSC Ensembl
Innerchr9:1870197..2658587hg19UCSC Ensembl
Innerchr9:1860197..2648587hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38788391
hg19788391
hg18788391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692357
Samples
Known GenesFLJ35024, SMARCA2, VLDLR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020530
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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