A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500082



Internal ID22558018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103085677..103094731hg38UCSC Ensembl
chr7:102726124..102735178hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389055
hg199055
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860212
Supporting Variants
Samples
Known GenesARMC10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500082
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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