A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997438



Internal ID18810288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236210757..237034862hg38UCSC Ensembl
Innerchr2:237119400..237943505hg19UCSC Ensembl
Innerchr2:236784139..237608244hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38824106
hg19824106
hg18824106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586954
Samples
Known GenesACKR3, ASB18, IQCA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997438
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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