A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514092



Internal ID20887443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44162601..44164600hg38UCSC Ensembl
chr17:42239969..42241968hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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