A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518003



Internal ID20891364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57534177..57620096hg38UCSC Ensembl
chr17:55611538..55697457hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3885920
hg1985920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037071
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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