A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5735



Internal ID15550574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:49430927..49475688hg38UCSC Ensembl
Outerchr7:49470523..49515284hg19UCSC Ensembl
Outerchr7:49441069..49485830hg18UCSC Ensembl
Outerchr7:49247784..49292545hg17UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3844762
hg1944762
hg1844762
hg1744762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8371
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)nsv5735
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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