A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141271



Internal ID18915932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84181948..84224848hg38UCSC Ensembl
Outerchr15:84850700..84893600hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3842901
hg1942901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992776
SamplesKWS2
Known GenesLOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141271
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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