A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503439



Internal ID20876694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21229968..21231847hg38UCSC Ensembl
chr17:21133281..21135160hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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