A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700628



Internal ID21222463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76170756..76173077hg38UCSC Ensembl
chr5:75466581..75468902hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg382322
hg192322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812991
Supporting Variants
Samples
Known GenesSV2C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700628
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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