A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582200



Internal ID18533795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87094919..87747090hg38UCSC Ensembl
Innerchr2:87322042..88046609hg19UCSC Ensembl
Innerchr2:87175553..87827724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38652172
hg19724568
hg18652172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009756
Supporting Variants
Samples
Known GenesLINC00152, 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)nssv3582200
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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