A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467157



Internal ID21124710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77451577..77451898hg38UCSC Ensembl
chr11:77162622..77162943hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994144
Samples
Known GenesPAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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