A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041440



Internal ID19130659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132906398..132947727hg38UCSC Ensembl
Innerchr12:133482984..133524313hg19UCSC Ensembl
Innerchr12:131993057..132034386hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3841330
hg1941330
hg1841330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526384
Samples
Known GenesZNF605
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041440
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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