A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3476



Internal ID15191518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:142116209..142149985hg38UCSC Ensembl
Outerchr6:142437346..142471122hg19UCSC Ensembl
Outerchr6:142479039..142512815hg18UCSC Ensembl
Outerchr6:142479039..142512815hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385967
hg195967
hg185967
hg175967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510
Supporting Variants
SamplesNA12878
Known GenesVTA1
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)nssv3476
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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