A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024435



Internal ID19113652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15134859..15269734hg38UCSC Ensembl
Innerchr7:15174484..15309359hg19UCSC Ensembl
Innerchr7:15141009..15275884hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38134876
hg19134876
hg18134876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643170
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024435
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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