A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505913



Internal ID20879187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38828625..38836701hg38UCSC Ensembl
chr17:36984878..36992954hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388077
hg198077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035303
Samples
Known GenesC17orf98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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