A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317769



Internal ID20850858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143535301..143769200hg38UCSC Ensembl
chr1:149029963..149263846hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38233900
hg19233884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv328n223
Supporting Variantsnssv18200731
Samples
Known GenesLOC101929780, NBPF23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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