A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957023



Internal ID18864380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:101582219..101582282hg38UCSC Ensembl
Outerchr3:101301063..101301126hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109535
Supporting Variants
SamplesKWS1
Known GenesPCNP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957023
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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