A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518945



Internal ID20892306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57773431..57776558hg38UCSC Ensembl
chr17:55850792..55853919hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383128
hg193128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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