A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998902



Internal ID19158439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:169184191..169473519hg38UCSC Ensembl
Innerchr2:170040701..170330029hg19UCSC Ensembl
Innerchr2:169748947..170038275hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38289329
hg19289329
hg18289329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729271
Samples
Known GenesLRP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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