A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656



Internal ID15550487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:21770779..21777054hg38UCSC Ensembl
Outerchr7:21810397..21816672hg19UCSC Ensembl
Outerchr7:21776922..21783197hg18UCSC Ensembl
Outerchr7:21583637..21589912hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386276
hg196276
hg186276
hg176276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8345
SamplesNA12156
Known GenesDNAH11
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)nsv5656
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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