A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439892



Internal ID22497762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103085711..103094645hg38UCSC Ensembl
chr7:102726158..102735092hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388935
hg198935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918526
Supporting Variants
Samples
Known GenesARMC10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439892
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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