A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585164



Internal ID6625482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9110101..9121072hg38UCSC Ensembl
Innerchr1:9110101..9121072hg38UCSC Ensembl
Outerchr1:9109975..9121195hg38UCSC Ensembl
chr1:9170160..9181131hg19UCSC Ensembl
Innerchr1:9170160..9181131hg19UCSC Ensembl
Outerchr1:9170034..9181254hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810972
hg1910972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9850191, essv9850190, essv9850189
SamplesHG04238, HG03772, HG02136
Known GenesGPR157
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585164
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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