A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561880



Internal ID334847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43113878..43113885hg38UCSC Ensembl
chr7:43153477..43153484hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg388
hg198
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996321
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561880
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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