A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335801



Internal ID20993354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218324673..218328946hg38UCSC Ensembl
chr2:219189396..219193669hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg384274
hg194274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085888
Samples
Known GenesPNKD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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