A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320170



Internal ID20853268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37849376..37850188hg38UCSC Ensembl
chr1:38315048..38315860hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202461
Samples
Known GenesMTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320170
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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