A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562494



Internal ID335448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113470041..113470977hg38UCSC Ensembl
chr7:113110096..113111032hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562494
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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