A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936999



Internal ID21357069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99520442..99520564hg38UCSC Ensembl
chr14:99986779..99986901hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183748
SamplesHG002
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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