A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555338



Internal ID328497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30471072..30471102hg38UCSC Ensembl
chr7:30510688..30510718hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3831
hg1931
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16995088
Samples
Known GenesNOD1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555338
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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