A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3578



Internal ID15538306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:126400414..126435958hg38UCSC Ensembl
Outerchr7:126040468..126076012hg19UCSC Ensembl
Outerchr7:125827704..125863248hg18UCSC Ensembl
Outerchr7:125634419..125669963hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3835545
hg1935545
hg1835545
hg1735545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5937
Supporting Variants
SamplesNA12878
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)nssv3578
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer