A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6161



Internal ID15537702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108179979..108192580hg38UCSC Ensembl
Outerchr7:107820423..107833024hg19UCSC Ensembl
Outerchr7:107607659..107620260hg18UCSC Ensembl
Outerchr7:107414374..107426975hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg388397
hg198397
hg188397
hg178397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894
Supporting Variants
SamplesNA12156
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)nssv6161
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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