A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173001



Internal ID15531587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59509698..59605717hg38UCSC Ensembl
Innerchr1:59975370..60071389hg19UCSC Ensembl
Innerchr1:59747958..59843977hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3896020
hg1996020
hg1896020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546317
Supporting Variants
SamplesHGDP01171
Known GenesFGGY
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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