A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9670



Internal ID15193447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:207523602..207564975hg38UCSC Ensembl
Outerchr1:207696947..207738320hg19UCSC Ensembl
Outerchr1:205763570..205804943hg18UCSC Ensembl
Outerchr1:204085342..204126715hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3841374
hg1941374
hg1841374
hg1741374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4232
Supporting Variants
SamplesNA18507
Known GenesCR1
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)nssv9670
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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