A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8529



Internal ID15535335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:95204237..95249443hg38UCSC Ensembl
Outerchr8:96216465..96261671hg19UCSC Ensembl
Outerchr8:96285641..96330847hg18UCSC Ensembl
Outerchr8:96285641..96330847hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3845207
hg1945207
hg1845207
hg1745207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315
Supporting Variants
SamplesNA12156
Known GenesC8orf37, C8orf69
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)nssv8529
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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