A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10182



Internal ID15542616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:108366618..108468532hg38UCSC Ensembl
Outerchr1:108909240..109011154hg19UCSC Ensembl
Outerchr1:108710763..108812677hg18UCSC Ensembl
Outerchr1:108621282..108723196hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38101915
hg19101915
hg18101915
hg17101915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2276
Supporting Variants
SamplesNA18956
Known GenesNBPF6
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)nssv10182
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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