A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620168



Internal ID7007041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28529033..28685462hg38UCSC Ensembl
chr9:28529031..28685460hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38156430
hg19156430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1465e214
Supporting Variantsessv13436662, essv13436657, essv13436658, essv13436660, essv13436659, essv13436661
SamplesNA07357, HG00243, NA20759, HG04195, HG04017, NA18865
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620168
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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