A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321677



Internal ID20854785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209778301..209779900hg38UCSC Ensembl
chr1:209951646..209953245hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057351
Samples
Known GenesTRAF3IP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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