A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318667



Internal ID20851759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74224701..74281500hg38UCSC Ensembl
chr1:74690385..74747184hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3856800
hg1956800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204411
Samples
Known GenesFPGT-TNNI3K, TNNI3K
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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