A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002684



Internal ID21912027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87118507..87124700hg38UCSC Ensembl
chr10:88878264..88884457hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg386194
hg196194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580442
Samples
Known GenesFAM35A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002684
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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