A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956240



Internal ID18871396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:173608338..173609237hg38UCSC Ensembl
Outerchr5:173035341..173036240hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127706
Supporting Variants
SamplesKWS1
Known GenesBOD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956240
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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