A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508229



Internal ID20881528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5240124..5253269hg38UCSC Ensembl
chr17:5143419..5156564hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3813146
hg1913146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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