A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1238n106



Internal ID20160595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72093624..72095859hg38UCSC Ensembl
chr15:72385965..72388200hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382236
hg192236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118588, nsv1121156, nsv1126137, nsv1129942
SamplesKWS1, KWS2
Known GenesMYO9A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1238n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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