A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335491



Internal ID20868683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6937301..6937606hg38UCSC Ensembl
chr1:6997361..6997666hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204329
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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