A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546621



Internal ID18401011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86882269..86882752hg38UCSC Ensembl
Outerchr10:86882210..86882788hg38UCSC Ensembl
Innerchr10:88642026..88642509hg19UCSC Ensembl
Outerchr10:88641967..88642545hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745368
Samples
Known GenesBMPR1A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546621
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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