A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435621



Internal ID22493491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37532368..37538068hg38UCSC Ensembl
chr8:37389886..37395586hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385701
hg195701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435621
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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