A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1878



Internal ID15546441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75055637..75067520hg38UCSC Ensembl
Outerchr16:75089535..75101418hg19UCSC Ensembl
Outerchr16:73647036..73658919hg18UCSC Ensembl
Outerchr16:73647036..73658919hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385910
hg195910
hg185910
hg175910
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10098
SamplesNA18956
Known GenesZNRF1
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)nsv1878
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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