A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035602



Internal ID18778133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110876295..111021655hg38UCSC Ensembl
Innerchr10:112636053..112781413hg19UCSC Ensembl
Innerchr10:112626043..112771403hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38145361
hg19145361
hg18145361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503950
Samples
Known GenesBBIP1, MIR4680, PDCD4, RPL13AP6, SHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035602
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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