A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3186



Internal ID15537914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:100581232..100600074hg38UCSC Ensembl
Outerchr3:100300076..100318918hg19UCSC Ensembl
Outerchr3:101782766..101801608hg18UCSC Ensembl
Outerchr3:101782766..101801608hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg386519
hg196519
hg186519
hg176519
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3920
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3186
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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