A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994092



Internal ID20561132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6512001..6514100hg38UCSC Ensembl
chr11:6533231..6535330hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440804
Supporting Variants
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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