A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504848



Internal ID22562792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28260618..28269409hg38UCSC Ensembl
chr7:28300237..28309028hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg388792
hg198792
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846797
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504848
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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