A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239946



Internal ID22044556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155357145..155357145hg38UCSC Ensembl
chr7:155149840..155149840hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839514
Samples
Known GenesBLACE
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239946
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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