A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9896540



Internal ID877191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33341155..33343580hg38UCSC Ensembl
Innerchr1:33341155..33343580hg38UCSC Ensembl
Outerchr1:33340896..33343872hg38UCSC Ensembl
chr1:33806756..33809181hg19UCSC Ensembl
Innerchr1:33806756..33809181hg19UCSC Ensembl
Outerchr1:33806497..33809473hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585684
Supporting Variants
SamplesHG00472
Known GenesPHC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9896540
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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