A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121291



Internal ID18918283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:73446587..73446651hg38UCSC Ensembl
Outerchr4:74312304..74312368hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970797, nssv3989183
SamplesKWS1, KWS2
Known GenesAFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121291
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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