A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7049



Internal ID15536815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:169623227..169669354hg38UCSC Ensembl
Outerchr3:169341015..169387142hg19UCSC Ensembl
Outerchr3:170823709..170869836hg18UCSC Ensembl
Outerchr3:170823717..170869844hg17UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3846128
hg1946128
hg1846128
hg1746128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4111
Supporting Variants
SamplesNA12156
Known GenesMECOM
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)nssv7049
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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