A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762595



Internal ID18958594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105442680..105442772hg38UCSC Ensembl
Outerchr14:105909017..105909109hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078210
Supporting Variants
SamplesKWP1
Known GenesMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762595
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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