A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502657



Internal ID20875903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104949873..104953051hg38UCSC Ensembl
chr14:105416210..105419388hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg383179
hg193179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2262n223
Supporting Variantsnssv18196939
Samples
Known GenesAHNAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502657
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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