A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910056



Internal ID22685266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121535916..121619133hg38UCSC Ensembl
chr7:121175970..121259187hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3883218
hg1983218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910056
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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