A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10098



Internal ID15542699
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 StatusS
Merged Variantsnsv1878
Supporting Variants
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)nssv10098
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer