A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10632897



Internal ID634713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114794993..114837510hg38UCSC Ensembl
chr2:115552570..115595087hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3842518
hg1942518
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3592057
Supporting Variants
SamplesHG03949
Known GenesDPP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10632897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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