A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325787



Internal ID20858919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210111301..210112500hg38UCSC Ensembl
chr1:210284646..210285845hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057327
Samples
Known GenesSYT14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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