A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034937



Internal ID18777469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152869077..153157810hg38UCSC Ensembl
Innerchr7:152566162..152854895hg19UCSC Ensembl
Innerchr7:152197095..152485828hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38288734
hg19288734
hg18288734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674276
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034937
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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