A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635448



Internal ID7022247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97627331..97638912hg38UCSC Ensembl
Innerchr14:97627331..97638912hg38UCSC Ensembl
Outerchr14:97626831..97639412hg38UCSC Ensembl
chr14:98093668..98105249hg19UCSC Ensembl
Innerchr14:98093668..98105249hg19UCSC Ensembl
Outerchr14:98093168..98105749hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811582
hg1911582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103760, essv15103759
SamplesHG00182, HG03850
Known GenesLOC100129345
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635448
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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