A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527024



Internal ID8421299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12164182..12207208hg38UCSC Ensembl
Innerchr1:12224239..12267265hg19UCSC Ensembl
Innerchr1:12146826..12189852hg18UCSC Ensembl
Innerchr1:12158505..12201531hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3843027
hg1943027
hg1843027
hg1743027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703399
Samples
Known GenesMIR4632, MIR7846, TNFRSF1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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