A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479224



Internal ID256754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44816243..44816331hg38UCSC Ensembl
chr7:44855842..44855930hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16995520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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