A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501338



Internal ID20874571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44126836..44142217hg38UCSC Ensembl
chr17:42204204..42219585hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3815382
hg1915382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035759
Samples
Known GenesC17orf53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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