A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497630



Internal ID20870838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42921844..42924015hg38UCSC Ensembl
chr17:41073861..41076032hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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