A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644137



Internal ID6684205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30454716..30456620hg38UCSC Ensembl
Innerchr19:30454716..30456620hg38UCSC Ensembl
Outerchr19:30454680..30456686hg38UCSC Ensembl
chr19:30945623..30947527hg19UCSC Ensembl
Innerchr19:30945623..30947527hg19UCSC Ensembl
Outerchr19:30945587..30947593hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381905
hg191905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16033394
SamplesHG02108
Known GenesZNF536
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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