A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958079



Internal ID18864072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:157099986..157110561hg38UCSC Ensembl
Outerchr5:156526997..156537572hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3810576
hg1910576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109742
Supporting Variants
SamplesKWS1
Known GenesHAVCR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958079
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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