A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351615



Internal ID22577284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62520193..62523120hg38UCSC Ensembl
chr11:62287665..62290592hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382928
hg192928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914598
Supporting Variants
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351615
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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