A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027214



Internal ID19116433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42323342..42353109hg38UCSC Ensembl
Innerchr7:42362941..42392708hg19UCSC Ensembl
Innerchr7:42329466..42359233hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3829768
hg1929768
hg1829768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6340n100
Supporting Variantsnssv3661217, nssv3661220, nssv3661218, nssv3752958, nssv3661219
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)nsv1027214
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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