A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329667



Internal ID20862820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31417401..31420600hg38UCSC Ensembl
chr1:31890248..31893447hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060387
Samples
Known GenesSERINC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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