A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519012



Internal ID20892373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55599601..55600900hg38UCSC Ensembl
chr17:53676962..53678261hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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