A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17858701



Internal ID22042344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2774017..2774017hg38UCSC Ensembl
chr6:2774251..2774251hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6256582
Supporting Variants
Samples
Known GenesWRNIP1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17858701
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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