A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435998



Internal ID22493868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1888350..1888477hg38UCSC Ensembl
chr7:1927986..1928113hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920101
Supporting Variants
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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