A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6083312



Internal ID9639813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37460968..37462158hg38UCSC Ensembl
chr4:37462590..37463780hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656828
Supporting Variants
SamplesNA19374
Known GenesC4orf19
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6083312
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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