A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955125



Internal ID19220730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44517029..44517087hg38UCSC Ensembl
Outerchr15:44809227..44809285hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127429
Supporting Variants
SamplesKWS1
Known GenesCTDSPL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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