A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978882



Internal ID20545922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12892765..12905611hg38UCSC Ensembl
chr10:12934765..12947611hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812847
hg1912847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446230
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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