A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6532



Internal ID15190646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31414561..31433391hg38UCSC Ensembl
Outerchr1:31887408..31906238hg19UCSC Ensembl
Outerchr1:31659995..31678825hg18UCSC Ensembl
Outerchr1:31556501..31575331hg17UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg388121
hg198121
hg188121
hg178121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7712
Supporting Variants
SamplesNA12156
Known GenesSERINC2
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)nssv6532
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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