A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4954



Internal ID15197409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165306927..165322006hg38UCSC Ensembl
Outerchr6:165720416..165735495hg19UCSC Ensembl
Outerchr6:165640406..165655485hg18UCSC Ensembl
Outerchr6:165690827..165705906hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3815080
hg1915080
hg1815080
hg1715080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5586
Supporting Variants
SamplesNA19129
Known GenesC6orf118
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)nssv4954
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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