A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2648



Internal ID15540462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:49678958..49706350hg38UCSC Ensembl
Outerchr7:49718554..49745946hg19UCSC Ensembl
Outerchr7:49689100..49716492hg18UCSC Ensembl
Outerchr7:49495815..49523207hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3827393
hg1927393
hg1827393
hg1727393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5736
Supporting Variants
SamplesNA18555
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)nssv2648
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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