A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10168819



Internal ID170635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161600533..161628390hg38UCSC Ensembl
chr1:161570323..161598180hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3827858
hg1927858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587732
Supporting Variants
SamplesNA19655
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10168819
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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