A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10994



Internal ID15192896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36340817..36374513hg38UCSC Ensembl
Outerchr19:36831719..36865415hg19UCSC Ensembl
Outerchr19:41523559..41557255hg18UCSC Ensembl
Outerchr19:41523559..41557255hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3833697
hg1933697
hg1833697
hg1733697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2474
Supporting Variants
SamplesNA15510
Known GenesZFP14
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)nssv10994
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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