A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674



Internal ID15545258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108186927..108195028hg38UCSC Ensembl
Outerchr7:107827371..107835472hg19UCSC Ensembl
Outerchr7:107614607..107622708hg18UCSC Ensembl
Outerchr7:107421322..107429423hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386962
hg196962
hg186962
hg176962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894
Supporting Variants
SamplesNA19240
Known GenesNRCAM
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)nssv674
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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