A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4357



Internal ID15192398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36313567..36358770hg38UCSC Ensembl
Outerchr19:36804469..36849672hg19UCSC Ensembl
Outerchr19:41496309..41541512hg18UCSC Ensembl
Outerchr19:41496309..41541512hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3845204
hg1945204
hg1845204
hg1745204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2474
Supporting Variants
SamplesNA12878
Known GenesLINC00665, ZFP14
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)nssv4357
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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