A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527585



Internal ID20900946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52302820..52315516hg38UCSC Ensembl
chr17:50380180..50392876hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3812697
hg1912697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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