A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525025



Internal ID15452318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:55255884..55278320hg38UCSC Ensembl
Innerchr2:55483020..55505456hg19UCSC Ensembl
Innerchr2:55336524..55358960hg18UCSC Ensembl
Innerchr2:55394671..55417107hg17UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3822437
hg1922437
hg1822437
hg1722437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701065
Samples
Known GenesMTIF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525025
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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