A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355267



Internal ID21012820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:50710337..51647226hg38UCSC Ensembl
chr2:50937475..51874364hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38936890
hg19936890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087167
Samples
Known GenesNRXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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