A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917063



Internal ID22692282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99488020..99488082hg38UCSC Ensembl
chr7:99085643..99085705hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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