A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707213



Internal ID21229011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72216137..72216231hg38UCSC Ensembl
chr8:73128372..73128466hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818163
Supporting Variants
Samples
Known GenesLOC392232
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707213
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.109375


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