A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643805



Internal ID7030562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16948582..16950259hg38UCSC Ensembl
Innerchr19:16948592..16950250hg38UCSC Ensembl
Outerchr19:16948573..16950269hg38UCSC Ensembl
chr19:17059392..17061069hg19UCSC Ensembl
Innerchr19:17059402..17061060hg19UCSC Ensembl
Outerchr19:17059383..17061079hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381678
hg191678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002867
SamplesNA19431
Known GenesCPAMD8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643805
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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