A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531876



Internal ID20905237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67657474..67657681hg38UCSC Ensembl
chr17:65653590..65653797hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037419
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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