A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11555782



Internal ID1557598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106170645..106178058hg38UCSC Ensembl
Innerchr4:106170668..106178035hg38UCSC Ensembl
Outerchr4:106170622..106178081hg38UCSC Ensembl
chr4:107091802..107099215hg19UCSC Ensembl
Innerchr4:107091825..107099192hg19UCSC Ensembl
Outerchr4:107091779..107099238hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg387414
hg197414
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601677
Supporting Variants
SamplesHG03779
Known GenesTBCK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11555782
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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