A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864743



Internal ID22639678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122337664..122341181hg38UCSC Ensembl
chr7:121977718..121981235hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383518
hg193518
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509608
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864743
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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