A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707756



Internal ID19006037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37545448..37605332hg38UCSC Ensembl
Innerchr10:37834376..37894260hg19UCSC Ensembl
Innerchr10:37874382..37934266hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3859885
hg1959885
hg1859885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041584
Supporting Variants
Samples
Known GenesMTRNR2L7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707756
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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