A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436651



Internal ID22494521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66901460..66901675hg38UCSC Ensembl
chr7:66366447..66366662hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436651
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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