A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10376



Internal ID15195736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:172054782..172079206hg38UCSC Ensembl
Outerchr3:171772572..171796996hg19UCSC Ensembl
Outerchr3:173255266..173279690hg18UCSC Ensembl
Outerchr3:173255274..173279698hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg388429
hg198429
hg188429
hg178429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4116
Supporting Variants
SamplesNA18956
Known GenesFNDC3B
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)nssv10376
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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