A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758



Internal ID15538486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135991307..136025933hg38UCSC Ensembl
Outerchr9:138883153..138917779hg19UCSC Ensembl
Outerchr9:138022974..138057600hg18UCSC Ensembl
Outerchr9:136109098..136143724hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385114
hg195114
hg185114
hg175114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6761
Supporting Variants
SamplesNA12878
Known GenesNACC2
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)nssv3758
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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