A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965240



Internal ID19246094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:149327058..149327298hg38UCSC Ensembl
Outerchr5:148706621..148706861hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130088
Supporting Variants
SamplesKWS2
Known GenesAFAP1L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965240
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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