A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440929



Internal ID21098482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98217201..98218700hg38UCSC Ensembl
chr10:99976958..99978457hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985789
Samples
Known GenesR3HCC1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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