A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324145



Internal ID20857270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35573301..35575700hg38UCSC Ensembl
chr1:36038902..36041301hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202425
Samples
Known GenesTFAP2E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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