A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436190



Internal ID22494060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69551587..69552909hg38UCSC Ensembl
chr7:69016573..69017895hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381323
hg191323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910254
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436190
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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