A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049238



Internal ID19138457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92015031..92065627hg38UCSC Ensembl
Innerchr13:92667284..92717880hg19UCSC Ensembl
Innerchr13:91465285..91515881hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3850597
hg1950597
hg1850597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525486
Samples
Known GenesGPC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049238
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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