A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318112



Internal ID20851203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177010612..177011589hg38UCSC Ensembl
chr1:176979748..176980725hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053774
Samples
Known GenesASTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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