A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450560



Internal ID21108113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13488699..13490974hg38UCSC Ensembl
chr10:13530699..13532974hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382276
hg192276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979028
Samples
Known GenesBEND7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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