A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585170



Internal ID6972694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9392634..9394487hg38UCSC Ensembl
Innerchr1:9392658..9394463hg38UCSC Ensembl
Outerchr1:9392610..9394511hg38UCSC Ensembl
chr1:9452693..9454546hg19UCSC Ensembl
Innerchr1:9452717..9454522hg19UCSC Ensembl
Outerchr1:9452669..9454570hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381854
hg191854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9850207
SamplesHG03199
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585170
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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