A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2656



Internal ID9624036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16681097..16799163hg38UCSC Ensembl
Innerchr1:17007592..17125658hg19UCSC Ensembl
Innerchr1:16880179..16998245hg18UCSC Ensembl
Innerchr1:16752898..16870964hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38118067
hg19118067
hg18118067
hg17118067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757725
Supporting Variants
SamplesNA18967
Known GenesESPNP, LOC729574, MIR3675, MST1L
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv2656
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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