A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439254



Internal ID21096807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14304707..14339526hg38UCSC Ensembl
chr10:14346706..14381525hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3834820
hg1934820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188895
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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