A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349844



Internal ID21007397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218315341..218319175hg38UCSC Ensembl
chr2:219180064..219183898hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg383835
hg193835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085887
Samples
Known GenesPNKD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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