A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494034



Internal ID21151587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61682601..61683700hg38UCSC Ensembl
chr14:62149319..62150418hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020370
Samples
Known GenesHIF1A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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