A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1582



Internal ID15198806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155182130..155219701hg38UCSC Ensembl
Outerchr1:155154606..155189492hg19UCSC Ensembl
Outerchr1:153421230..153456116hg18UCSC Ensembl
Outerchr1:151967679..152002565hg17UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg386112
hg196112
hg186112
hg176112
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2988
Supporting Variants
SamplesNA19240
Known GenesGBAP1, MIR92B, MTX1, MUC1, THBS3, TRIM46
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)nssv1582
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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