A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602804



Internal ID6643060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157112338..157116548hg38UCSC Ensembl
Innerchr4:157112338..157116548hg38UCSC Ensembl
Outerchr4:157112151..157116751hg38UCSC Ensembl
chr4:158033490..158037700hg19UCSC Ensembl
Innerchr4:158033490..158037700hg19UCSC Ensembl
Outerchr4:158033303..158037903hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659909, essv11659904, essv11659908, essv11659905, essv11659910, essv11659907, essv11659906
SamplesHG01089, HG01205, HG01054, HG01286, HG01101, HG01356, HG01162
Known GenesGLRB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602804
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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