A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031395



Internal ID19120617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103176214..103228551hg38UCSC Ensembl
Innerchr7:102816661..102868998hg19UCSC Ensembl
Innerchr7:102603897..102656234hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3852338
hg1952338
hg1852338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656126
Samples
Known GenesDPY19L2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031395
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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