A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438362



Internal ID21095915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125734501..125735300hg38UCSC Ensembl
chr10:127423070..127423869hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978647
Samples
Known GenesC10orf137
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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