A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477067



Internal ID254661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66151468..66155240hg38UCSC Ensembl
chr7:65616455..65620227hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997630
Samples
Known GenesCRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477067
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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