A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181598



Internal ID20748638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7357953..7358466hg38UCSC Ensembl
chr10:7399915..7400428hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441395
Supporting Variants
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00022


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