A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580855



Internal ID18532450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131213210..131543555hg38UCSC Ensembl
Innerchr2:131970783..132301128hg19UCSC Ensembl
Innerchr2:131687253..132017598hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38330346
hg19330346
hg18330346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000842
Supporting Variants
Samples
Known GenesCCDC74A, LINC01120, LOC150776, LOC401010, LOC440910, MIR4784, MZT2A, POTEE, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580855
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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