A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659249



Internal ID1870785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155602057..155604461hg38UCSC Ensembl
Innerchr4:155602107..155604411hg38UCSC Ensembl
Outerchr4:155601993..155604525hg38UCSC Ensembl
chr4:156523209..156525613hg19UCSC Ensembl
Innerchr4:156523259..156525563hg19UCSC Ensembl
Outerchr4:156523145..156525677hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602762
Supporting Variants
SamplesHG01767
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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