A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3911



Internal ID15548568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:95605756..95651540hg38UCSC Ensembl
Outerchr3:95324600..95370384hg19UCSC Ensembl
Outerchr3:96807290..96853074hg18UCSC Ensembl
Outerchr3:96807290..96853074hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3845785
hg1945785
hg1845785
hg1745785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7016
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)nsv3911
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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