A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024807



Internal ID19114024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42322533..42353109hg38UCSC Ensembl
Innerchr7:42362132..42392708hg19UCSC Ensembl
Innerchr7:42328657..42359233hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3830577
hg1930577
hg1830577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6340n100
Supporting Variantsnssv3752957, nssv3752956, nssv3661215
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)nsv1024807
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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