A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111786



Internal ID19264138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25686253..25687253hg38UCSC Ensembl
Outerchr15:25931400..25932400hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1180n106
Supporting Variantsnssv3964694
SamplesKWS2
Known GenesATP10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111786
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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