A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321085



Internal ID20854187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119381211..119394004hg38UCSC Ensembl
chr1:119923834..119936627hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3812794
hg1912794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200364
Samples
Known GenesHAO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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