A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10531



Internal ID15542267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1186981..1200542hg38UCSC Ensembl
Outerchr7:1226617..1240178hg19UCSC Ensembl
Outerchr7:1193143..1206704hg18UCSC Ensembl
Outerchr7:999858..1013419hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3813302
hg1913302
hg1813302
hg1713302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613
Supporting Variants
SamplesNA18956
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)nssv10531
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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