A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337951



Internal ID20995504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2245551..2254786hg38UCSC Ensembl
chr2:2249323..2258558hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg389236
hg199236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083800
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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