A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv636



Internal ID15545232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:56675990..56708740hg38UCSC Ensembl
Outerchr7:56743683..56776433hg19UCSC Ensembl
Outerchr7:56711177..56743927hg18UCSC Ensembl
Outerchr7:56517892..56550642hg17UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3832751
hg1932751
hg1832751
hg1732751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5759
Supporting Variants
SamplesNA19240
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)nssv636
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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