A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585734



Internal ID6973255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36352807..36353928hg38UCSC Ensembl
Innerchr1:36352858..36353877hg38UCSC Ensembl
Outerchr1:36352756..36353979hg38UCSC Ensembl
chr1:36818408..36819529hg19UCSC Ensembl
Innerchr1:36818459..36819478hg19UCSC Ensembl
Outerchr1:36818357..36819580hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9907438
SamplesHG01354
Known GenesSTK40
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585734
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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