A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785993



Internal ID18815206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6703997..6739489hg38UCSC Ensembl
Innerchr9:6703997..6739489hg19UCSC Ensembl
Innerchr9:6693997..6729489hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835493
hg1935493
hg1835493
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891544
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785993
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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