A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529330



Internal ID20902691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56879096..56883252hg38UCSC Ensembl
chr17:54956457..54960613hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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