A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563019



Internal ID335957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91857662..91893869hg38UCSC Ensembl
chr7:91486976..91523183hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3836208
hg1936208
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002126
Samples
Known GenesMTERF
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563019
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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