A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082698



Internal ID15589198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34670442..34696590hg38UCSC Ensembl
Innerchr7:34710054..34736202hg19UCSC Ensembl
Innerchr7:34676579..34702727hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3826149
hg1926149
hg1826149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606615
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)nssv1082698
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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