A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10352



Internal ID15542446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:75405587..75422999hg38UCSC Ensembl
Outerchr3:75454738..75472150hg19UCSC Ensembl
Outerchr3:75537428..75554840hg18UCSC Ensembl
Outerchr3:75537428..75554840hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3811318
hg1911318
hg1811318
hg1711318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3883
Supporting Variants
SamplesNA18956
Known GenesFAM86DP
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)nssv10352
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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