A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9863683



Internal ID1471127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15674986..15683392hg38UCSC Ensembl
Innerchr1:15674986..15683392hg38UCSC Ensembl
Outerchr1:15674867..15683476hg38UCSC Ensembl
chr1:16001481..16009887hg19UCSC Ensembl
Innerchr1:16001481..16009887hg19UCSC Ensembl
Outerchr1:16001362..16009971hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585316
Supporting Variants
SamplesHG01357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9863683
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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