A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449631



Internal ID22507501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89132296..89137219hg38UCSC Ensembl
chr6:89842015..89846938hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449631
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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