A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917161



Internal ID22692380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129973516..129974664hg38UCSC Ensembl
chr7:129613356..129614504hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917161
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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