A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14766421



Internal ID2642135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61957562..61981680hg38UCSC Ensembl
chr13:62531695..62555813hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3824119
hg1924119
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632351
Supporting Variants
SamplesHG02337
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14766421
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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