A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7222



Internal ID15536642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:904169..920604hg38UCSC Ensembl
Outerchr16:954169..970604hg19UCSC Ensembl
Outerchr16:894170..910605hg18UCSC Ensembl
Outerchr16:894170..910605hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385820
hg195820
hg185820
hg175820
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1705
Supporting Variants
SamplesNA12156
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)nssv7222
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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