A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7897



Internal ID15535967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:174581890..174615606hg38UCSC Ensembl
Outerchr3:174299680..174333396hg19UCSC Ensembl
Outerchr3:175782374..175816090hg18UCSC Ensembl
Outerchr3:175782382..175816098hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3833717
hg1933717
hg1833717
hg1733717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4125
Supporting Variants
SamplesNA12156
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)nssv7897
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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