A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818163



Internal ID21263501
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 StatusM
Merged Variants
Supporting Variantsnssv13707213
Samples
Known GenesLOC392232
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818163
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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