A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031202



Internal ID19120423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62369829hg38UCSC Ensembl
Innerchr7:61063962..61814080hg19UCSC Ensembl
Innerchr7:61067904..61451515hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381288593
hg19750119
hg18383612
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661535, nssv3661536
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)nsv1031202
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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