A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004756



Internal ID21914099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31845756..31854405hg38UCSC Ensembl
chr10:32134684..32143333hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388650
hg198650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580750
Samples
Known GenesARHGAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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