A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341550



Internal ID20999103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31911245..31915929hg38UCSC Ensembl
chr2:32136314..32140998hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg384685
hg194685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085282
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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