A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6286791



Internal ID9264194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157112341..157116537hg38UCSC Ensembl
chr4:158033493..158037689hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384197
hg194197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661593
Supporting Variants
SamplesHG01356
Known GenesGLRB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6286791
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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