A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035914



Internal ID19125133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122393588..122435198hg38UCSC Ensembl
Innerchr10:124153104..124194714hg19UCSC Ensembl
Innerchr10:124143094..124184704hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3841611
hg1941611
hg1841611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv987n100
Supporting Variantsnssv3503157
Samples
Known GenesMIR3941, PLEKHA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035914
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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