A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048725



Internal ID18791256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46459209hg38UCSC Ensembl
Innerchr10:47090539..47138582hg19UCSC Ensembl
Innerchr10:46510545..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3848040
hg1948044
hg1848044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv818n100
Supporting Variantsnssv3518393
Samples
Known GenesHNRNPA1P33, LINC00842
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048725
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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