A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442002



Internal ID22499872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:46860948..46862567hg38UCSC Ensembl
chr8:47772570..47774189hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442002
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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