A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460723



Internal ID21118276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77995654..77996519hg38UCSC Ensembl
chr11:77706700..77707565hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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