A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017907



Internal ID19107124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62997085hg38UCSC Ensembl
Innerchr7:61063962..62457463hg19UCSC Ensembl
Innerchr7:61067904..62094898hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381915849
hg191393502
hg181026995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6386n100
Supporting Variantsnssv3752988
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)nsv1017907
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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