A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9397



Internal ID15193662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:209897229..209925152hg38UCSC Ensembl
Outerchr1:210070574..210098497hg19UCSC Ensembl
Outerchr1:208137197..208165120hg18UCSC Ensembl
Outerchr1:206458969..206486892hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3827924
hg1927924
hg1827924
hg1727924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4354
Supporting Variants
SamplesNA18517
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)nssv9397
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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