A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1595



Internal ID15546158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70713112..70754601hg38UCSC Ensembl
Outerchr15:71005451..71046940hg19UCSC Ensembl
Outerchr15:68792505..68833994hg18UCSC Ensembl
Outerchr15:68792505..68833994hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3841490
hg1941490
hg1841490
hg1741490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1260, nssv5562
SamplesNA19240, NA19129
Known GenesUACA
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)nsv1595
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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