A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113725



Internal ID18931411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:72164903..72164975hg38UCSC Ensembl
Outerchr15:72457244..72457316hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969794
SamplesKWS2
Known GenesGRAMD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113725
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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