A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992818



Internal ID20559858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73162360..73162586hg38UCSC Ensembl
chr11:72873405..72873631hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00197


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