A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762347



Internal ID19312181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:126260420..126260492hg38UCSC Ensembl
Outerchr3:125979263..125979335hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078951
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762347
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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