A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120322



Internal ID19285351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:81514046..81514167hg38UCSC Ensembl
Outerchr1:81979731..81979852hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv116n106
Supporting Variantsnssv3961890
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120322
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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