A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022740



Internal ID19111958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132783362..132833582hg38UCSC Ensembl
Innerchr8:133795608..133845827hg19UCSC Ensembl
Innerchr8:133864790..133915009hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3850221
hg1950220
hg1850220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7319n100
Supporting Variantsnssv3691558
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022740
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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