A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6527098



Internal ID9504501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23930426..24035232hg38UCSC Ensembl
Outerchr1:23930055..24035602hg38UCSC Ensembl
Innerchr1:24256916..24361722hg19UCSC Ensembl
Outerchr1:24256545..24362092hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38105548
hg19105548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662136
Supporting Variants
SamplesHG01519
Known GenesPNRC2, SRSF10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6527098
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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