A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356287



Internal ID22581956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050711..74051276hg38UCSC Ensembl
chr11:73761756..73762321hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915720
Supporting Variants
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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