A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452315



Internal ID21109868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:815765..1016488hg38UCSC Ensembl
chr10:861705..1062428hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38200724
hg19200724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183545
Samples
Known GenesGTPBP4, LARP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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