A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619750



Internal ID7006624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14287295..14291408hg38UCSC Ensembl
Innerchr9:14287345..14291356hg38UCSC Ensembl
Outerchr9:14287194..14291509hg38UCSC Ensembl
chr9:14287294..14291407hg19UCSC Ensembl
Innerchr9:14287344..14291355hg19UCSC Ensembl
Outerchr9:14287193..14291508hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13407120, essv13407118, essv13407112, essv13407116, essv13407121, essv13407110, essv13407117, essv13407111, essv13407114, essv13407122, essv13407115, essv13407119, essv13407113
SamplesHG00358, HG00187, HG00318, NA20759, HG02477, HG02450, NA12546, NA20522, HG00383, NA11881, HG01260, HG00339, NA11843
Known GenesNFIB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619750
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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