A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635449



Internal ID7022248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97663580..97674744hg38UCSC Ensembl
Innerchr14:97664080..97674244hg38UCSC Ensembl
Outerchr14:97662580..97675744hg38UCSC Ensembl
chr14:98129917..98141081hg19UCSC Ensembl
Innerchr14:98130417..98140581hg19UCSC Ensembl
Outerchr14:98128917..98142081hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811165
hg1911165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103761, essv15103768, essv15103773, essv15103774, essv15103764, essv15103769, essv15103763, essv15103772, essv15103765, essv15103775, essv15103766, essv15103771, essv15103776, essv15103767, essv15103762, essv15103770
SamplesHG03298, HG03280, HG03193, HG02888, HG03452, HG02461, NA18516, HG02555, HG02817, NA20351, HG02580, HG03419, HG03039, HG02971, HG02465, NA19346
Known GenesLOC100129345
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635449
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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