A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532001



Internal ID20905362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69272433..69321096hg38UCSC Ensembl
chr17:67268574..67317237hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3848664
hg1948664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037620
Samples
Known GenesABCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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