A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049824



Internal ID19139043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74788910..74816448hg38UCSC Ensembl
Innerchr9:77403826..77431364hg19UCSC Ensembl
Innerchr9:76593646..76621184hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3827539
hg1927539
hg1827539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696363
Samples
Known GenesTRPM6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049824
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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