A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333404



Internal ID20866580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29224725..29226719hg38UCSC Ensembl
chr1:29551237..29553231hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203556
Samples
Known GenesMECR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333404
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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