A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6201695



Internal ID8852865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37850376..37855632hg38UCSC Ensembl
Outerchr19:37850005..37856002hg38UCSC Ensembl
Innerchr19:38341016..38346272hg19UCSC Ensembl
Outerchr19:38340645..38346642hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662482
Supporting Variants
SamplesHG00309
Known GenesLOC100631378
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6201695
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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