A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027574



Internal ID19116793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102010780..102106045hg38UCSC Ensembl
Innerchr7:101654060..101749325hg19UCSC Ensembl
Innerchr7:101440780..101536045hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3895266
hg1995266
hg1895266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656104
Samples
Known GenesCUX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027574
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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