A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053631



Internal ID19142850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97160497..97233890hg38UCSC Ensembl
Innerchr12:97554275..97627668hg19UCSC Ensembl
Innerchr12:96078406..96151799hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3873394
hg1973394
hg1873394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524833
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)nsv1053631
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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