A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587514



Internal ID6974937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150878846..150879354hg38UCSC Ensembl
Innerchr1:150878896..150879304hg38UCSC Ensembl
Outerchr1:150878715..150879485hg38UCSC Ensembl
chr1:150851322..150851830hg19UCSC Ensembl
Innerchr1:150851372..150851780hg19UCSC Ensembl
Outerchr1:150851191..150851961hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10145195, essv10145194, essv10145193, essv10145190, essv10145192, essv10145189, essv10145191
SamplesNA21135, NA21103, NA21129, NA21122, NA21119, NA19118, NA19035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587514
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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