A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8357



Internal ID15535507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:34359469..34404413hg38UCSC Ensembl
Outerchr7:34399081..34444025hg19UCSC Ensembl
Outerchr7:34365606..34410550hg18UCSC Ensembl
Outerchr7:34172321..34217265hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3844945
hg1944945
hg1844945
hg1744945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5692
Supporting Variants
SamplesNA12156
Known GenesNPSR1-AS1
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)nssv8357
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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