A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439390



Internal ID22497260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94225990..94226084hg38UCSC Ensembl
chr8:95238218..95238312hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439390
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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