A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924810



Internal ID22700037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128751153..128751215hg38UCSC Ensembl
chr7:128391207..128391269hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435687
Samples
Known GenesCALU
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924810
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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