A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664464



Internal ID9583883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36349114..36355770hg38UCSC Ensembl
Outerchr19:36348743..36356140hg38UCSC Ensembl
Innerchr19:36840016..36846672hg19UCSC Ensembl
Outerchr19:36839645..36847042hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg387398
hg197398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv638e199
Supporting Variantsessv5631430, essv5437162, essv5428157, essv5849337, essv5428604, essv6347092, essv5919278, essv6503515, essv6416338, essv6173415, essv6128805, essv6067394, essv5429492
SamplesHG01356, HG01359, HG01456, HG01350, HG01492, HG01365, HG01360, HG01497, HG01357, HG01494, HG01113, HG01491, HG01378
Known GenesZFP14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664464
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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