A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10541



Internal ID15542257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:49676023..49687450hg38UCSC Ensembl
Outerchr7:49715619..49727046hg19UCSC Ensembl
Outerchr7:49686165..49697592hg18UCSC Ensembl
Outerchr7:49492880..49504307hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3811428
hg1911428
hg1811428
hg1711428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5736
Supporting Variants
SamplesNA18956
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)nssv10541
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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