A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321556



Internal ID20854663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204141201..204143500hg38UCSC Ensembl
chr1:204110329..204112628hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057000
Samples
Known GenesETNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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