A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037608



Internal ID20604649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69191056..69234238hg38UCSC Ensembl
chr17:67187197..67230379hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3843183
hg1943183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524913
Supporting Variants
Samples
Known GenesABCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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