A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329729



Internal ID20862882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155877087..155877585hg38UCSC Ensembl
chr1:155846878..155847376hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052103
Samples
Known GenesSYT11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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