A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890847



Internal ID458109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89633664..89638659hg38UCSC Ensembl
Innerchr10:89633667..89638657hg38UCSC Ensembl
Outerchr10:89633662..89638662hg38UCSC Ensembl
chr10:91393421..91398416hg19UCSC Ensembl
Innerchr10:91393424..91398414hg19UCSC Ensembl
Outerchr10:91393419..91398419hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384996
hg194996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624165
Supporting Variants
SamplesHG00145
Known GenesPANK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890847
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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