A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957689



Internal ID18861166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:151149937..151149999hg38UCSC Ensembl
Outerchr5:150529498..150529560hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128201
Supporting Variants
SamplesKWS1
Known GenesANXA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957689
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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