A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6611



Internal ID15190567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:54615870..54663322hg38UCSC Ensembl
Outerchr1:55081543..55128995hg19UCSC Ensembl
Outerchr1:54854131..54901583hg18UCSC Ensembl
Outerchr1:54793564..54841016hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3847453
hg1947453
hg1847453
hg1747453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv910
Supporting Variants
SamplesNA12156
Known GenesACOT11, FAM151A, MROH7, MROH7-TTC4
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)nssv6611
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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