A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318758



Internal ID20851850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66755226..66772638hg38UCSC Ensembl
chr1:67220909..67238321hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3817413
hg1917413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062626
Samples
Known GenesTCTEX1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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