A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440216



Internal ID22498086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87345722..87346386hg38UCSC Ensembl
chr7:86975038..86975702hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915095
Supporting Variants
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440216
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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