A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10145189



Internal ID5600640
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587514
Supporting Variants
SamplesNA19035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10145189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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