A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510182



Internal ID20883498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100982381..100983195hg38UCSC Ensembl
chr14:101448718..101449532hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016490
Samples
Known GenesSNORD114-22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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