A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11554949



Internal ID1556765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106102808..106127774hg38UCSC Ensembl
chr4:107023965..107048931hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3824967
hg1924967
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601673
Supporting Variants
SamplesHG01342
Known GenesTBCK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11554949
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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