A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440348



Internal ID21097901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88739737..88768190hg38UCSC Ensembl
chr10:90499494..90527947hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3828454
hg1928454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984293
Samples
Known GenesLIPK, LIPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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