A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024261



Internal ID18766794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130226209..130323135hg38UCSC Ensembl
Innerchr7:129866049..129962975hg19UCSC Ensembl
Innerchr7:129653285..129750211hg18UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3896927
hg1996927
hg1896927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662185
Samples
Known GenesCPA2, CPA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024261
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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