A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964214



Internal ID19230445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:55363302..55364902hg38UCSC Ensembl
Outerchr15:55655500..55657100hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120995
Supporting Variants
SamplesKWS2
Known GenesCCPG1, DYX1C1-CCPG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964214
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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