A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558625



Internal ID331683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42563614..42574342hg38UCSC Ensembl
chr7:42603213..42613941hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3810729
hg1910729
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558625
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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