A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017676



Internal ID19106893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:52864446..53282831hg38UCSC Ensembl
Innerchr7:52932139..53350524hg19UCSC Ensembl
Innerchr7:52899633..53318018hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38418386
hg19418386
hg18418386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661280
Samples
Known GenesPOM121L12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017676
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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