A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517234



Internal ID15444527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15259117..15267170hg38UCSC Ensembl
Innerchr1:15585613..15593666hg19UCSC Ensembl
Innerchr1:15458200..15466253hg18UCSC Ensembl
Innerchr1:15330919..15338972hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg388054
hg198054
hg188054
hg178054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678288, nssv654089, nssv691051, nssv669267
Samples
Known GenesFHAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517234
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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