A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891542



Internal ID19185938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6673700..6739489hg38UCSC Ensembl
Outerchr9:6673465..6744721hg38UCSC Ensembl
Innerchr9:6673700..6739489hg19UCSC Ensembl
Outerchr9:6673465..6744721hg19UCSC Ensembl
Innerchr9:6663700..6729489hg18UCSC Ensembl
Outerchr9:6663465..6734721hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3871257
hg1971257
hg1871257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799042, essv25799700, essv25798976, essv25782640, essv25783718, essv25798760, essv25797680, essv25799130, essv25798054
Samples
Known GenesKDM4C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891542
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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