A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858169



Internal ID22633104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32788597..32819622hg38UCSC Ensembl
chr10:33077525..33108550hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3831026
hg1931026
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459813
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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