A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462292



Internal ID21119845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74972936..74973567hg38UCSC Ensembl
chr11:74683981..74684612hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38632
hg19632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993632
Samples
Known GenesSPCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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