A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430719



Internal ID22488589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75389377..75396883hg38UCSC Ensembl
chr9:78004293..78011799hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387507
hg197507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430719
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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