A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317914



Internal ID20851004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161579455..161661271hg38UCSC Ensembl
chr1:161549245..161631061hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881817
hg1981817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053271
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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