A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419739



Internal ID22477609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132527934..132528044hg38UCSC Ensembl
chr6:132849073..132849183hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419739
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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