A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610731



Internal ID20983802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165245624..165246986hg38UCSC Ensembl
chr6:165659113..165660475hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381363
hg191363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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