A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6774



Internal ID15190404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18731508..18763602hg38UCSC Ensembl
Outerchr19:18842318..18874412hg19UCSC Ensembl
Outerchr19:18703318..18735412hg18UCSC Ensembl
Outerchr19:18703318..18735412hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387341
hg197341
hg187341
hg177341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2433
Supporting Variants
SamplesNA12156
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)nssv6774
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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