A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501391



Internal ID22559329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63884541..63886540hg38UCSC Ensembl
chr7:63344919..63346918hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501391
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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