A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490903



Internal ID268152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105102271..105102329hg38UCSC Ensembl
chr7:104742718..104742776hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003077
Samples
Known GenesKMT2E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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