A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463883



Internal ID21121436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74972166..74978167hg38UCSC Ensembl
chr11:74683211..74689212hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386002
hg196002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993631
Samples
Known GenesSPCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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