A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10176



Internal ID15195936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18710556..18714245hg38UCSC Ensembl
Outerchr19:18821366..18825055hg19UCSC Ensembl
Outerchr19:18682366..18686055hg18UCSC Ensembl
Outerchr19:18682366..18686055hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387726
hg197726
hg187726
hg177726
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2431
Supporting Variants
SamplesNA18956
Known GenesCRTC1
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)nssv10176
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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