A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499039



Internal ID20872255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35050007..35050897hg38UCSC Ensembl
chr17:33377026..33377916hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035082
Samples
Known GenesRAD51L3-RFFL, RFFL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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