A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512167



Internal ID20885498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102637217..102638675hg38UCSC Ensembl
chr14:103103554..103105012hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015677
Samples
Known GenesRCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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