A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989988



Internal ID7061231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87941591..87941662hg38UCSC Ensembl
chr6:88651309..88651380hg19UCSC Ensembl
chr6:88708028..88708099hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3575134
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989988
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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