A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005520



Internal ID21914863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12906756..12912726hg38UCSC Ensembl
chr10:12948756..12954726hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385971
hg195971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585721
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005520
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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