A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13905513



Internal ID3907329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95946719..95999705hg38UCSC Ensembl
chr10:97706476..97759462hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3852987
hg1952987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624287
Supporting Variants
SamplesNA18924
Known GenesENTPD1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13905513
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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