A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524685



Internal ID20898046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62404151..62412276hg38UCSC Ensembl
chr17:60481512..60489637hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg388126
hg198126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037175
Samples
Known GenesEFCAB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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