A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987929



Internal ID20554969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131637573..131721664hg38UCSC Ensembl
chr11:131507467..131591558hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3884092
hg1984092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472429
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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