A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441340



Internal ID22499210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123704494..123704549hg38UCSC Ensembl
chr7:123344548..123344603hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914081
Supporting Variants
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441340
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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