A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503999



Internal ID20877257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44300201..44306200hg38UCSC Ensembl
chr17:42377569..42383568hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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