A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321813



Internal ID20854921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25173901..25405600hg38UCSC Ensembl
chr1:25500392..25732091hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38231700
hg19231700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202825
Samples
Known GenesC1orf63, RHCE, RHD, SYF2, TMEM50A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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