A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1573



Internal ID15546136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66093065..66111620hg38UCSC Ensembl
Outerchr15:66385403..66403958hg19UCSC Ensembl
Outerchr15:64172457..64191012hg18UCSC Ensembl
Outerchr15:64172457..64191012hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811768
hg1911768
hg1811768
hg1711768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10932, nssv9517, nssv4157, nssv2110, nssv10058, nssv5560, nssv6636
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA19129
Known GenesMEGF11
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)nsv1573
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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