A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341170



Internal ID20998723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109560528..109563356hg38UCSC Ensembl
chr2:110318105..110320933hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075361
Samples
Known GenesSEPT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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