A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561272



Internal ID334256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23740705..23744875hg38UCSC Ensembl
chr7:23780324..23784494hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384171
hg194171
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994540
Samples
Known GenesSTK31
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561272
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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