A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509367



Internal ID22567317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82542112..82544236hg38UCSC Ensembl
chr7:82171428..82173552hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382125
hg192125
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509367
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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