A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326046



Internal ID20859180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176006698..176020302hg38UCSC Ensembl
chr1:175975834..175989438hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3813605
hg1913605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053710
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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