A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1604



Internal ID15198781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44640957..44687581hg38UCSC Ensembl
Outerchr20:43269598..43316222hg19UCSC Ensembl
Outerchr20:42703012..42749636hg18UCSC Ensembl
Outerchr20:42703012..42749636hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3846625
hg1946625
hg1846625
hg1746625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3390
Supporting Variants
SamplesNA19240
Known GenesADA, LOC79015
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)nssv1604
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