A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv715292



Internal ID15662562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59583022..59583728hg38UCSC Ensembl
Innerchr1:60048694..60049400hg19UCSC Ensembl
Innerchr1:59821282..59821988hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38707
hg19707
hg18707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546326
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)nssv715292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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