A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661587



Internal ID15051553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87203604..87476787hg38UCSC Ensembl
Innerchr2:87430727..87776306hg19UCSC Ensembl
Innerchr2:87284238..87557421hg18UCSC Ensembl
Innerchr2:87342385..87615568hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38273184
hg19345580
hg18273184
hg17273184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516958
Supporting Variants
Samples
Known GenesLINC00152
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661587
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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