A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974137



Internal ID19236206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77470854..77503452hg38UCSC Ensembl
Outerchr5:76766679..76799277hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3832599
hg1932599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123962
Supporting Variants
SamplesKWS2
Known GenesWDR41
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974137
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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