A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857356



Internal ID22040999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72618933..72618933hg38UCSC Ensembl
chr6:73328661..73328661hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857356
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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