A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9750831



Internal ID18725077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102693301..102693651hg38UCSC Ensembl
Outerchr14:102693300..102693656hg38UCSC Ensembl
Innerchr14:103159638..103159988hg19UCSC Ensembl
Outerchr14:103159637..103159993hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552084
Supporting Variants
Samples
Known GenesRCOR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9750831
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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