A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524208



Internal ID15104815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231077778..231171079hg38UCSC Ensembl
Innerchr2:231942492..232035793hg19UCSC Ensembl
Innerchr2:231650736..231744037hg18UCSC Ensembl
Innerchr2:231767997..231861298hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3893302
hg1993302
hg1893302
hg1793302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700095
Samples
Known GenesHTR2B, PSMD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524208
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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