A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619979



Internal ID20993050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118818152..118834820hg38UCSC Ensembl
chr6:119139315..119155983hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3816669
hg1916669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138800
Samples
Known GenesMCM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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