A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13946406



Internal ID4111998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116636787..116638143hg38UCSC Ensembl
Innerchr10:116636797..116638133hg38UCSC Ensembl
Outerchr10:116636777..116638153hg38UCSC Ensembl
chr10:118396298..118397654hg19UCSC Ensembl
Innerchr10:118396308..118397644hg19UCSC Ensembl
Outerchr10:118396288..118397664hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624661
Supporting Variants
SamplesHG03731
Known GenesPNLIPRP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13946406
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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