A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv607



Internal ID15545264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:896162..910548hg38UCSC Ensembl
Outerchr7:935799..950185hg19UCSC Ensembl
Outerchr7:902325..916711hg18UCSC Ensembl
Outerchr7:709040..723426hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3813901
hg1913901
hg1813901
hg1713901
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611
Supporting Variants
SamplesNA19240
Known GenesADAP1, GET4
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)nssv607
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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