A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992776



Internal ID18881128
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 StatusS
Merged Variantsnsv1141271
Supporting Variants
SamplesKWS2
Known GenesLOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992776
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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