A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021890



Internal ID19111108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61089312..62335035hg38UCSC Ensembl
Innerchr7:61072037..61779286hg19UCSC Ensembl
Innerchr7:61075979..61416721hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381245724
hg19707250
hg18340743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6383n100
Supporting Variantsnssv3661555
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)nsv1021890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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