A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1705



Internal ID15546268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:890581..923385hg38UCSC Ensembl
Outerchr16:940581..973385hg19UCSC Ensembl
Outerchr16:880582..913386hg18UCSC Ensembl
Outerchr16:880582..913386hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385820
hg195820
hg185820
hg175820
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7222, nssv4185
SamplesNA12156, NA12878
Known GenesLMF1
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)nsv1705
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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