A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616328



Internal ID20989399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99544600..99545323hg38UCSC Ensembl
chr6:99992476..99993199hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147642
Samples
Known GenesCCNC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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