A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512412



Internal ID18810693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122369174..122442149hg38UCSC Ensembl
Innerchr10:124128690..124201665hg19UCSC Ensembl
Innerchr10:124118680..124191655hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3872976
hg1972976
hg1872976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042640
Supporting Variants
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512412
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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