A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499824



Internal ID20873048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101043380..101044695hg38UCSC Ensembl
chr14:101509717..101511032hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016493
Samples
Known GenesMIR1185-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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