A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2408



Internal ID15200285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:9142047..9154649hg38UCSC Ensembl
Outerchr19:9252723..9265325hg19UCSC Ensembl
Outerchr19:9113723..9126325hg18UCSC Ensembl
Outerchr19:9113723..9126325hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812603
hg1912603
hg1812603
hg1712603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2209
SamplesNA18555
Known GenesZNF317
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)nsv2408
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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