A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516991



Internal ID20890352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81614225..81616601hg38UCSC Ensembl
chr17:79581251..79583627hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382377
hg192377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039187
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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