A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7836



Internal ID15536028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:88560076..88605400hg38UCSC Ensembl
Outerchr3:88609226..88654550hg19UCSC Ensembl
Outerchr3:88691916..88737240hg18UCSC Ensembl
Outerchr3:88691916..88737240hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3845325
hg1945325
hg1845325
hg1745325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3906
Supporting Variants
SamplesNA12156
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)nssv7836
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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