A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582333



Internal ID18880614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87861756hg38UCSC Ensembl
Innerchr2:87373881..88161275hg19UCSC Ensembl
Innerchr2:87227392..87942390hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38714999
hg19787395
hg18714999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004209
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, PLGLB1, PLGLB2, RGPD1, RGPD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582333
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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