A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034891



Internal ID19124111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62589040..63259826hg38UCSC Ensembl
Innerchr7:62049418..62720204hg19UCSC Ensembl
Innerchr7:61686853..62357639hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38670787
hg19670787
hg18670787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3661872, nssv3661868, nssv3661871, nssv3661869, nssv3661870
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)nsv1034891
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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