A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715282



Internal ID15662552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59583022..59583611hg38UCSC Ensembl
Innerchr1:60048694..60049283hg19UCSC Ensembl
Innerchr1:59821282..59821871hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38590
hg19590
hg18590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546324
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)nssv715282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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