A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330850



Internal ID20864008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161601401..161629000hg38UCSC Ensembl
chr1:161571191..161598790hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3827600
hg1927600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv421n223
Supporting Variantsnssv18201274
Samples
Known GenesFCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330850
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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