A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496729



Internal ID20869932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102822626..102957863hg38UCSC Ensembl
chr14:103288963..103424200hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38135238
hg19135238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193461
Samples
Known GenesAMN, CDC42BPB, TRAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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