A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586958



Internal ID6711654
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008172
Supporting Variants
SamplesHuRef
Known GenesFGGY
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586958
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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