A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324533



Internal ID20857661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15159663..15167868hg38UCSC Ensembl
chr1:15486159..15494364hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg388206
hg198206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200423
Samples
Known GenesC1orf195, TMEM51
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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