A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176



Internal ID15201073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:158985583..159016778hg38UCSC Ensembl
Outerchr1:158955373..158986568hg19UCSC Ensembl
Outerchr1:157221997..157253192hg18UCSC Ensembl
Outerchr1:155768446..155799641hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3831196
hg1931196
hg1831196
hg1731196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3433
SamplesNA12878
Known GenesIFI16
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)nsv3176
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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