A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489176



Internal ID266464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88044516..88045087hg38UCSC Ensembl
chr7:87673831..87674402hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002043
Samples
Known GenesADAM22
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489176
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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