A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606616



Internal ID16047339
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 StatusM
Merged Variants
Supporting Variantsnssv1082699
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)nsv606616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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