A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3569737



Internal ID7041119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36650943..36651053hg38UCSC Ensembl
chr4:36652565..36652675hg19UCSC Ensembl
chr4:36328960..36329070hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38111
hg19111
hg18111
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006741
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3569737
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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