A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331808



Internal ID20864975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173321796..173327834hg38UCSC Ensembl
chr1:173290935..173296973hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg386039
hg196039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201030
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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