A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504722



Internal ID22562665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2032476..2084806hg38UCSC Ensembl
chr7:2072111..2124441hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3852331
hg1952331
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846446
Supporting Variants
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504722
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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