A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324235



Internal ID20857360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212829001..212840800hg38UCSC Ensembl
chr1:213002343..213014142hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3811800
hg1911800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv524n223
Supporting Variantsnssv18057705
Samples
Known GenesC1orf227
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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