A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7041



Internal ID15190137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:154313497..154345052hg38UCSC Ensembl
Outerchr3:154031286..154062841hg19UCSC Ensembl
Outerchr3:155513980..155545535hg18UCSC Ensembl
Outerchr3:155513988..155545543hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387886
hg197886
hg187886
hg177886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4073
Supporting Variants
SamplesNA12156
Known GenesDHX36, GPR149
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)nssv7041
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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