A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970948



Internal ID19218183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24881526..24881619hg38UCSC Ensembl
Outerchr15:25126673..25126766hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131176
Supporting Variants
SamplesKWS1
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970948
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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