A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11501499



Internal ID3791531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73567388..73580796hg38UCSC Ensembl
chr4:74433105..74446513hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3813409
hg1913409
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600997
Supporting Variants
SamplesHG03439
Known GenesRASSF6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11501499
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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