A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037347



Internal ID19126566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46481242hg38UCSC Ensembl
Innerchr10:47068215..47153919hg19UCSC Ensembl
Innerchr10:46488221..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3885400
hg1985705
hg1885705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv812n100
Supporting Variantsnssv3705910, nssv3705911
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037347
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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