A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839311



Internal ID22022954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138941911..138941911hg38UCSC Ensembl
chr7:138626657..138626657hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239823
Supporting Variants
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839311
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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