A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2734



Internal ID15195153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:137849427..137883180hg38UCSC Ensembl
Outerchr6:138170564..138204317hg19UCSC Ensembl
Outerchr6:138212257..138246010hg18UCSC Ensembl
Outerchr6:138212257..138246010hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386228
hg196228
hg186228
hg176228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493
Supporting Variants
SamplesNA18555
Known GenesLOC100130476, TNFAIP3
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)nssv2734
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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