A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11138371



Internal ID6046322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128595415..128596224hg38UCSC Ensembl
Innerchr3:128595418..128596221hg38UCSC Ensembl
Outerchr3:128595412..128596227hg38UCSC Ensembl
chr3:128314258..128315067hg19UCSC Ensembl
Innerchr3:128314261..128315064hg19UCSC Ensembl
Outerchr3:128314255..128315070hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597710
Supporting Variants
SamplesNA19445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11138371
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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