A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3102



Internal ID15540873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:82686526..82720981hg38UCSC Ensembl
Outerchr3:82735677..82770132hg19UCSC Ensembl
Outerchr3:82818367..82852822hg18UCSC Ensembl
Outerchr3:82818367..82852822hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385558
hg195558
hg185558
hg175558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3894
Supporting Variants
SamplesNA18555
Known Genes
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)nssv3102
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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