A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322075



Internal ID20855184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213205465..213217272hg38UCSC Ensembl
chr1:213378808..213390615hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3811808
hg1911808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057744
Samples
Known GenesRPS6KC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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