A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9436



Internal ID15193701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165301680..165333728hg38UCSC Ensembl
Outerchr6:165715169..165747217hg19UCSC Ensembl
Outerchr6:165635159..165667207hg18UCSC Ensembl
Outerchr6:165685580..165717628hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3832049
hg1932049
hg1832049
hg1732049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5586
Supporting Variants
SamplesNA18517
Known GenesC6orf118, PDE10A
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)nssv9436
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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