A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582175



Internal ID18533770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87023361..87661069hg38UCSC Ensembl
Innerchr2:87250484..87960588hg19UCSC Ensembl
Innerchr2:87103995..87741703hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38637709
hg19710105
hg18637709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002590
Supporting Variants
Samples
Known GenesLINC00152, LOC285074, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582175
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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