A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020297



Internal ID19109516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62909444hg38UCSC Ensembl
Innerchr7:61063962..62369822hg19UCSC Ensembl
Innerchr7:61067904..62007257hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381828208
hg191305861
hg18939354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6386n100
Supporting Variantsnssv3661550, nssv3661552, nssv3661548, nssv3661549, nssv3661551
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)nsv1020297
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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