A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620703



Internal ID6660884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74531823..74532491hg38UCSC Ensembl
Innerchr9:74531835..74532479hg38UCSC Ensembl
Outerchr9:74531811..74532503hg38UCSC Ensembl
chr9:77146739..77147407hg19UCSC Ensembl
Innerchr9:77146751..77147395hg19UCSC Ensembl
Outerchr9:77146727..77147419hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13525036, essv13525038, essv13525039, essv13525035, essv13525037
SamplesHG03126, NA18977, HG02283, HG03539, HG02343
Known GenesMIR6130, RORB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620703
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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