A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481755



Internal ID259224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126019312..126910121hg38UCSC Ensembl
chr7:125659366..126550175hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38890810
hg19890810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002514
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481755
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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