A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032135



Internal ID19121357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48253507..48374557hg38UCSC Ensembl
Innerchr7:48293104..48414154hg19UCSC Ensembl
Innerchr7:48263650..48384700hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38121051
hg19121051
hg18121051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661257
Samples
Known GenesABCA13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032135
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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