A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4152



Internal ID15538879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43886826..43902554hg38UCSC Ensembl
Outerchr15:44179024..44194752hg19UCSC Ensembl
Outerchr15:41966316..41982044hg18UCSC Ensembl
Outerchr15:41966316..41982044hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg386398
hg196398
hg186398
hg176398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1515
Supporting Variants
SamplesNA12878
Known GenesFRMD5
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)nssv4152
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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