A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9911



Internal ID15539994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:108179219..108194243hg38UCSC Ensembl
Outerchr7:107819664..107834687hg19UCSC Ensembl
Outerchr7:107606900..107621923hg18UCSC Ensembl
Outerchr7:107413615..107428638hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387302
hg197302
hg187302
hg177302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894
Supporting Variants
SamplesNA18507
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)nssv9911
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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