A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501632



Internal ID20874869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35921063..35922202hg38UCSC Ensembl
chr17:34248067..34249206hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035148
Samples
Known GenesRDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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