A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994088



Internal ID20561128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65070610..65071117hg38UCSC Ensembl
chr11:64838082..64838589hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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