A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444637



Internal ID22502507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40294986..40295170hg38UCSC Ensembl
chr8:40152505..40152689hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444637
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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