A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6995



Internal ID15190183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13323369..13355052hg38UCSC Ensembl
Outerchr3:13364869..13396552hg19UCSC Ensembl
Outerchr3:13339869..13371552hg18UCSC Ensembl
Outerchr3:13339869..13371552hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg387756
hg197756
hg187756
hg177756
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3706
Supporting Variants
SamplesNA12156
Known GenesNUP210
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)nssv6995
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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