A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635423



Internal ID7022222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96385068..96403803hg38UCSC Ensembl
chr14:96851405..96870140hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818736
hg1918736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103569, essv15103568, essv15103567, essv15103565, essv15103566
SamplesHG03900, HG04035, HG03672, HG03949, HG03686
Known GenesAK7, GSKIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635423
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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