A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813651



Internal ID21258989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170191519..170191708hg38UCSC Ensembl
chr6:170506743..170506932hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813651
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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