A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453878



Internal ID21111431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113876906..113877389hg38UCSC Ensembl
chr10:115636665..115637148hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977673
Samples
Known GenesNHLRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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