A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316136



Internal ID20849214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73502781..73567033hg38UCSC Ensembl
chr1:73968464..74032716hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3864253
hg1964253
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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