A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554250



Internal ID327446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34709300..34799476hg38UCSC Ensembl
chr4:34710922..34801098hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3890177
hg1990177
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554250
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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