A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447434



Internal ID21104987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107066643..107086094hg38UCSC Ensembl
chr10:108826401..108845852hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3819452
hg1919452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977617
Samples
Known GenesSORCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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