A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502891



Internal ID20876140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5500601..5501100hg38UCSC Ensembl
chr17:5403921..5404420hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036889
Samples
Known GenesLOC728392
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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