A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436706



Internal ID22494576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9517295..9517504hg38UCSC Ensembl
chr6:9517528..9517737hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436706
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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