A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467888



Internal ID21125441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77278947..77285437hg38UCSC Ensembl
chr11:76989992..76996482hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386491
hg196491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994135
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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