A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082699



Internal ID15589199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34771298..34788335hg38UCSC Ensembl
Innerchr7:34810910..34827947hg19UCSC Ensembl
Innerchr7:34777435..34794472hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3817038
hg1917038
hg1817038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606616
Supporting Variants
Samples
Known GenesNPSR1, NPSR1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1082699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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