A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4088



Internal ID15202076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:201917968..201929082hg38UCSC Ensembl
Outerchr1:201887096..201898210hg19UCSC Ensembl
Outerchr1:200153719..200164833hg18UCSC Ensembl
Outerchr1:198618753..198629867hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386307
hg196307
hg186307
hg176307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2739
SamplesNA18555
Known GenesLMOD1
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)nsv4088
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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