A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583006



Internal ID18881287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:167171248..167215737hg38UCSC Ensembl
Innerchr2:168027758..168072247hg19UCSC Ensembl
Innerchr2:167736004..167780493hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3844490
hg1944490
hg1844490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015022
Supporting Variants
Samples
Known GenesXIRP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583006
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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