A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327207



Internal ID20860344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182248597..182254270hg38UCSC Ensembl
chr1:182217732..182223405hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385674
hg195674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054664
Samples
Known GenesLOC400799
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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