A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7037



Internal ID15190141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136298616..136331707hg38UCSC Ensembl
Outerchr3:136017458..136050549hg19UCSC Ensembl
Outerchr3:137500148..137533239hg18UCSC Ensembl
Outerchr3:137500156..137533247hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3833092
hg1933092
hg1833092
hg1733092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4025
Supporting Variants
SamplesNA12156
Known GenesPCCB
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)nssv7037
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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