A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5624



Internal ID15197130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89601681..89628517hg38UCSC Ensembl
Outerchr16:89668089..89694925hg19UCSC Ensembl
Outerchr16:88195590..88222426hg18UCSC Ensembl
Outerchr16:88195590..88222426hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg386328
hg196328
hg186328
hg176328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1929
Supporting Variants
SamplesNA19129
Known GenesDPEP1
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)nssv5624
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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