A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123815



Internal ID18939688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87022552..87022604hg38UCSC Ensembl
Outerchr4:87943704..87943756hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2845n106
Supporting Variantsnssv3973975
SamplesKWS2
Known GenesAFF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123815
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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