A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7801



Internal ID15189377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:170999097..171003832hg38UCSC Ensembl
Outerchr1:170968238..170972973hg19UCSC Ensembl
Outerchr1:169234862..169239597hg18UCSC Ensembl
Outerchr1:167699896..167704631hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg386102
hg196102
hg186102
hg176102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3487
Supporting Variants
SamplesNA12156
Known GenesMROH9
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)nssv7801
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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