A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839000



Internal ID22022643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73864137..73864137hg38UCSC Ensembl
chr7:73278467..73278467hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6245404
Supporting Variants
Samples
Known GenesWBSCR28
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839000
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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