A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13408049



Internal ID1936233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15419572..15430882hg38UCSC Ensembl
Innerchr9:15419572..15430882hg38UCSC Ensembl
Outerchr9:15419316..15431143hg38UCSC Ensembl
chr9:15419570..15430880hg19UCSC Ensembl
Innerchr9:15419570..15430880hg19UCSC Ensembl
Outerchr9:15419314..15431141hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3811311
hg1911311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619779
Supporting Variants
SamplesHG01802
Known GenesSNAPC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13408049
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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