A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517904



Internal ID20891265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57656391..57663797hg38UCSC Ensembl
chr17:55733752..55741158hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387407
hg197407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037078
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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