A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510237



Internal ID20883554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42789474..42791359hg38UCSC Ensembl
chr17:40941492..40943377hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381886
hg191886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035653
Samples
Known GenesWNK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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