A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005772



Internal ID19094989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4058193hg38UCSC Ensembl
Innerchr3:4087787..4099877hg19UCSC Ensembl
Innerchr3:4062787..4074877hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3812091
hg1912091
hg1812091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4645n100
Supporting Variantsnssv3739562, nssv3739561, nssv3739560, nssv3590419, nssv3590418, nssv3590420, nssv3739563, nssv3590421, nssv3590423, nssv3590422
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)nsv1005772
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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