A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330157



Internal ID20863311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117060716..117061162hg38UCSC Ensembl
chr1:117603338..117603784hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051833
Samples
Known GenesTTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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