A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502073



Internal ID22560013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140427398..140429149hg38UCSC Ensembl
chr7:140127198..140128949hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381752
hg191752
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502073
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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