A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523663



Internal ID20897024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69238044..69243780hg38UCSC Ensembl
chr17:67234185..67239921hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385737
hg195737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037613
Samples
Known GenesABCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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