A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007635



Internal ID19096854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185983043..186083155hg38UCSC Ensembl
Innerchr2:186847770..186947882hg19UCSC Ensembl
Innerchr2:186556015..186656127hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38100113
hg19100113
hg18100113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4131n100
Supporting Variantsnssv3729299
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007635
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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