A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352563



Internal ID21010116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69903201..69904900hg38UCSC Ensembl
chr2:70130333..70132032hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088906
Samples
Known GenesSNRNP27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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