A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485867



Internal ID263248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37730544..37851461hg38UCSC Ensembl
chr7:37770146..37891063hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38120918
hg19120918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994722
Samples
Known GenesGPR141, NME8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485867
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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