A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034546



Internal ID19123768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137147516..137174057hg38UCSC Ensembl
Innerchr7:136832263..136858804hg19UCSC Ensembl
Innerchr7:136482803..136509344hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3826542
hg1926542
hg1826542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664240
Samples
Known GenesLOC349160
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034546
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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