A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766538



Internal ID19308321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:135273327..135273416hg38UCSC Ensembl
Outerchr5:134609017..134609106hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078825
Supporting Variants
SamplesKWP1
Known GenesC5orf66
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766538
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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