A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355496



Internal ID21013049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38562201..38563900hg38UCSC Ensembl
chr2:38789343..38791042hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086369
Samples
Known GenesHNRNPLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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