A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670730



Internal ID9936835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5749939..5751516hg38UCSC Ensembl
chr9:5749939..5751516hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381578
hg191578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1320e199
Supporting Variantsessv5569871, essv6172116, essv6574859
SamplesNA19471, NA19982, NA19434
Known GenesKIAA1432
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670730
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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