A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122311



Internal ID18905985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24631863..24632003hg38UCSC Ensembl
Outerchr1:24958354..24958494hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970518
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122311
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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