A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812867



Internal ID21258205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169956976..169957078hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812867
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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