A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10151922



Internal ID153738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154185111..154188897hg38UCSC Ensembl
Innerchr1:154185111..154188897hg38UCSC Ensembl
Outerchr1:154184848..154189254hg38UCSC Ensembl
chr1:154157587..154161373hg19UCSC Ensembl
Innerchr1:154157587..154161373hg19UCSC Ensembl
Outerchr1:154157324..154161730hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383787
hg193787
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587601
Supporting Variants
SamplesHG02881
Known GenesTPM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10151922
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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