A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036071



Internal ID18778602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14310809..14337577hg38UCSC Ensembl
Innerchr10:14352808..14379576hg19UCSC Ensembl
Innerchr10:14392814..14419582hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3826769
hg1926769
hg1826769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv677n100
Supporting Variantsnssv3503316
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036071
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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