A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003080



Internal ID21912423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13062481..13065183hg38UCSC Ensembl
chr10:13104481..13107183hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593482
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003080
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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