A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316101



Internal ID20849178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27370335..27376901hg38UCSC Ensembl
chr1:27696826..27703393hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386567
hg196568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203501
Samples
Known GenesFCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316101
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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