A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031379



Internal ID19120601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62865123hg38UCSC Ensembl
Innerchr7:61063962..62325501hg19UCSC Ensembl
Innerchr7:61067904..61962936hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381783887
hg191261540
hg18895033
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661547, nssv3661546
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)nsv1031379
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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