A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322058



Internal ID20855167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114119342..114127124hg38UCSC Ensembl
chr1:114661964..114669746hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg387783
hg197783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051625
Samples
Known GenesSYT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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