A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5941



Internal ID15196746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:9192267..9223982hg38UCSC Ensembl
Outerchr3:9233951..9265666hg19UCSC Ensembl
Outerchr3:9208951..9240666hg18UCSC Ensembl
Outerchr3:9208951..9240666hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg387564
hg197564
hg187564
hg177564
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3690
Supporting Variants
SamplesNA19129
Known GenesSRGAP3, SRGAP3-AS3
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)nssv5941
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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