A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005635



Internal ID19094852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162394665..162426448hg38UCSC Ensembl
Innerchr3:162112453..162144236hg19UCSC Ensembl
Innerchr3:163595147..163626930hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3831784
hg1931784
hg1831784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607949, nssv3607950, nssv3607948
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)nsv1005635
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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