A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979997



Internal ID19241337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166683488..166683566hg38UCSC Ensembl
Outerchr5:166110493..166110571hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117422
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979997
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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