A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520156



Internal ID20893517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63725614..63725932hg38UCSC Ensembl
chr17:61802974..61803292hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037253
Samples
Known GenesSTRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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