A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234905



Internal ID20801945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87714707..87733072hg38UCSC Ensembl
chr7:87344023..87362388hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3818366
hg1918366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612025
Supporting Variants
Samples
Known GenesRUNDC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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