A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668150



Internal ID15058116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32855000..32914507hg38UCSC Ensembl
Innerchr1:33320601..33380108hg19UCSC Ensembl
Innerchr1:33093188..33152695hg18UCSC Ensembl
Innerchr1:32989694..33049201hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3859508
hg1959508
hg1859508
hg1759508
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516302
Supporting Variants
Samples
Known GenesFNDC5, HPCA, S100PBP, TMEM54
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668150
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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