A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530195



Internal ID20903556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69483201..69492502hg38UCSC Ensembl
chr17:67479342..67488643hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389302
hg199302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n223
Supporting Variantsnssv18037641
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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