A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785896



Internal ID19178422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70953639..70978694hg38UCSC Ensembl
Innerchr15:71245978..71271033hg19UCSC Ensembl
Innerchr15:69033032..69058087hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825056
hg1925056
hg1825056
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892710
Supporting Variants
Samples
Known GenesLRRC49
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785896
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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