A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1766



Internal ID15199643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:85412470..85445537hg38UCSC Ensembl
Outerchr1:85878153..85911220hg19UCSC Ensembl
Outerchr1:85650741..85683808hg18UCSC Ensembl
Outerchr1:85590174..85623241hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg386370
hg196370
hg186370
hg176370
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7335
SamplesNA12156
Known GenesDDAH1
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)nsv1766
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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