A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109754



Internal ID18939020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:180639273..180639409hg38UCSC Ensembl
Outerchr5:180066273..180066409hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958094
SamplesKWS1
Known GenesFLT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109754
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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