A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705848



Internal ID21227645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178793844..178793915hg38UCSC Ensembl
chr5:178220845..178220916hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705848
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.25


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