A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019062



Internal ID19108279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42322533..42361414hg38UCSC Ensembl
Innerchr7:42362132..42401013hg19UCSC Ensembl
Innerchr7:42328657..42367538hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3838882
hg1938882
hg1838882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6341n100
Supporting Variantsnssv3661216
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019062
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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