A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16100936



Internal ID6757580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56327053..56338394hg38UCSC Ensembl
Innerchr19:56327054..56338394hg38UCSC Ensembl
Outerchr19:56327053..56338395hg38UCSC Ensembl
chr19:56838422..56849763hg19UCSC Ensembl
Innerchr19:56838423..56849763hg19UCSC Ensembl
Outerchr19:56838422..56849764hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3811342
hg1911342
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644863
Supporting Variants
SamplesNA20868
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16100936
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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