A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602291



Internal ID20975362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106775148..106778022hg38UCSC Ensembl
chr6:107223023..107225897hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382875
hg192875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136887
Samples
Known GenesLOC100422737
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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