A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503927



Internal ID22561870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129956290..129965544hg38UCSC Ensembl
chr7:129596130..129605384hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg389255
hg199255
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503927
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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