A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620390



Internal ID7007261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36257629..36267537hg38UCSC Ensembl
Innerchr9:36257672..36267495hg38UCSC Ensembl
Outerchr9:36257587..36267580hg38UCSC Ensembl
chr9:36257626..36267534hg19UCSC Ensembl
Innerchr9:36257669..36267492hg19UCSC Ensembl
Outerchr9:36257584..36267577hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg389909
hg199909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13460321
SamplesHG01815
Known GenesGNE
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620390
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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