A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8371



Internal ID15535493
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 StatusS
Merged Variantsnsv5735
Supporting Variants
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)nssv8371
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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