A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998184



Internal ID18811034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152675973..153414946hg38UCSC Ensembl
Innerchr3:152393762..153132735hg19UCSC Ensembl
Innerchr3:153876452..154615425hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38738974
hg19738974
hg18738974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741543
Samples
Known GenesP2RY1, RAP2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998184
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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