A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528



Internal ID15538256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:51525796..51545544hg38UCSC Ensembl
Outerchr7:51593493..51613241hg19UCSC Ensembl
Outerchr7:51560987..51580735hg18UCSC Ensembl
Outerchr7:51367702..51387450hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3819749
hg1919749
hg1819749
hg1719749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5741
Supporting Variants
SamplesNA12878
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)nssv3528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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