A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410201



Internal ID22468071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136804050..136804112hg38UCSC Ensembl
chr6:137125188..137125250hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897133
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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