A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656138



Internal ID15046104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:126383591..126744960hg38UCSC Ensembl
Innerchr12:126868137..127229506hg19UCSC Ensembl
Innerchr12:125434090..125795459hg18UCSC Ensembl
Innerchr12:125393017..125754386hg17UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38361370
hg19361370
hg18361370
hg17361370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515762
Supporting Variants
Samples
Known GenesLINC00943, LINC00944, LOC100128554
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656138
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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