A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892646



Internal ID19183466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30648195..30672369hg38UCSC Ensembl
Outerchr15:30626045..30675803hg38UCSC Ensembl
Innerchr15:30940398..30964572hg19UCSC Ensembl
Outerchr15:30918248..30968006hg19UCSC Ensembl
Innerchr15:28727690..28751864hg18UCSC Ensembl
Outerchr15:28705540..28755298hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3849759
hg1949759
hg1849759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785940, essv25800769, essv25797175, essv25778340
Samples
Known GenesARHGAP11B, LOC100288637
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892646
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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