A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892710



Internal ID19183530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70953639..70978694hg38UCSC Ensembl
Outerchr15:70953639..70978694hg38UCSC Ensembl
Innerchr15:71245978..71271033hg19UCSC Ensembl
Outerchr15:71245978..71271033hg19UCSC Ensembl
Innerchr15:69033032..69058087hg18UCSC Ensembl
Outerchr15:69033032..69058087hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825056
hg1925056
hg1825056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785896
Samples
Known GenesLRRC49
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892710
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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