A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699596



Internal ID21221435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76984513..76984611hg38UCSC Ensembl
chr5:76280338..76280436hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699596
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.444444


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