A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788753



Internal ID18823865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5200714..5291710hg38UCSC Ensembl
Innerchr9:5200714..5291710hg19UCSC Ensembl
Innerchr9:5190714..5281710hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3890997
hg1990997
hg1890997
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891538
Supporting Variants
Samples
Known GenesINSL4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788753
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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