A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030687



Internal ID19119906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34361654..34438508hg38UCSC Ensembl
Innerchr7:34401266..34478120hg19UCSC Ensembl
Innerchr7:34367791..34444645hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3876855
hg1976855
hg1876855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643402
Samples
Known GenesNPSR1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030687
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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