A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1180n106



Internal ID22795008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25686249..25687253hg38UCSC Ensembl
chr15:25931396..25932400hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120696, nsv1111786, nsv1142607, nsv1121145
SamplesKWS2, KWS1
Known GenesATP10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1180n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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