A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473683



Internal ID21131236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60389922..60390727hg38UCSC Ensembl
chr11:60157395..60158200hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992503
Samples
Known GenesMS4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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