A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715446



Internal ID15662716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59583184..59584019hg38UCSC Ensembl
Innerchr1:60048856..60049691hg19UCSC Ensembl
Innerchr1:59821444..59822279hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38836
hg19836
hg18836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546346
Supporting Variants
Samples
Known GenesFGGY
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv715446
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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