A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316835



Internal ID20849917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204080368..204082114hg38UCSC Ensembl
chr1:204049496..204051242hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056999
Samples
Known GenesSOX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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