A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030968



Internal ID19120188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56542963..56863185hg38UCSC Ensembl
Innerchr7:56610656..56930878hg19UCSC Ensembl
Innerchr7:56578150..56898372hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38320223
hg19320223
hg18320223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752976
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)nsv1030968
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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