A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995982



Internal ID15581483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131523273..131697432hg38UCSC Ensembl
Innerchr2:132280846..132455005hg19UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38174160
hg19174160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483103
Supporting Variants
Samples
Known GenesCCDC74A, LINC01087, POTEKP, RNU6-81P
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995982
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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