A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6150



Internal ID15537713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93771061..93799840hg38UCSC Ensembl
Outerchr7:93400373..93429152hg19UCSC Ensembl
Outerchr7:93238309..93267088hg18UCSC Ensembl
Outerchr7:93045024..93073803hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3828780
hg1928780
hg1828780
hg1728780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848
Supporting Variants
SamplesNA12156
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)nssv6150
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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