A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706247



Internal ID19004528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121675623..121696088hg38UCSC Ensembl
Innerchr10:123435137..123455602hg19UCSC Ensembl
Innerchr10:123425127..123445592hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3820466
hg1920466
hg1820466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036503
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3706247
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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