A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891544



Internal ID18839254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6703997..6739489hg38UCSC Ensembl
Outerchr9:6703997..6739489hg38UCSC Ensembl
Innerchr9:6703997..6739489hg19UCSC Ensembl
Outerchr9:6703997..6739489hg19UCSC Ensembl
Innerchr9:6693997..6729489hg18UCSC Ensembl
Outerchr9:6693997..6729489hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835493
hg1935493
hg1835493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785993
Samples
Known GenesKDM4C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891544
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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