A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477615



Internal ID255189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27497665..27507668hg38UCSC Ensembl
chr7:27537284..27547287hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3810004
hg1910004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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