A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361595



Internal ID22587264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13047389..13051809hg38UCSC Ensembl
chr10:13089389..13093809hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384421
hg194421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921009
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361595
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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