A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1696



Internal ID15194293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152874051..152888733hg38UCSC Ensembl
Outerchr7:152571136..152585818hg19UCSC Ensembl
Outerchr7:152202069..152216751hg18UCSC Ensembl
Outerchr7:152008784..152023466hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3814683
hg1914683
hg1814683
hg1714683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6008
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)nssv1696
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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