A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008172



Internal ID6720282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:59582990..59586726hg38UCSC Ensembl
Innerchr1:60048662..60052398hg19UCSC Ensembl
Innerchr1:59821250..59824986hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg383737
hg193737
hg183737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586958
SamplesHuRef
Known GenesFGGY
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008172
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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