A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503866



Internal ID18802147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33112644..33140973hg38UCSC Ensembl
Innerchr12:33265578..33293907hg19UCSC Ensembl
Innerchr12:33156845..33185174hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3828330
hg1928330
hg1828330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035521
Supporting Variants
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)nssv3503866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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