A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505336



Internal ID20878604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1887421..1931491hg38UCSC Ensembl
chr17:1790715..1834785hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3844071
hg1944071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034764
Samples
Known GenesRPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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