A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779077



Internal ID18824173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:62191858..62221432hg38UCSC Ensembl
Innerchr1:62657530..62687104hg19UCSC Ensembl
Innerchr1:62430118..62459692hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3829575
hg1929575
hg1829575
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893612
Supporting Variants
Samples
Known GenesL1TD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779077
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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