A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7821



Internal ID15189357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:68030107..68063644hg38UCSC Ensembl
Outerchr3:68079257..68112794hg19UCSC Ensembl
Outerchr3:68161947..68195484hg18UCSC Ensembl
Outerchr3:68161947..68195484hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385891
hg195891
hg185891
hg175891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3861
Supporting Variants
SamplesNA12156
Known GenesFAM19A1
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)nssv7821
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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