A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13618676



Internal ID6093495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124310392..124312406hg38UCSC Ensembl
Innerchr9:124310392..124312406hg38UCSC Ensembl
Outerchr9:124310100..124312663hg38UCSC Ensembl
chr9:127072671..127074685hg19UCSC Ensembl
Innerchr9:127072671..127074685hg19UCSC Ensembl
Outerchr9:127072379..127074942hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621720
Supporting Variants
SamplesNA19473
Known GenesNEK6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13618676
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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