A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10767



Internal ID15195345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:78955245..78987712hg38UCSC Ensembl
Outerchr10:80715002..80747469hg19UCSC Ensembl
Outerchr10:80385008..80417475hg18UCSC Ensembl
Outerchr10:80385008..80417475hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387024
hg197024
hg187024
hg177024
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7343
Supporting Variants
SamplesNA18956
Known GenesZMIZ1-AS1
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)nssv10767
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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