A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507773



Internal ID22565722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54019671..54021870hg38UCSC Ensembl
chr7:54087364..54089563hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507773
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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