A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021700



Internal ID19110918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:42324206..42349475hg38UCSC Ensembl
Innerchr7:42363805..42389074hg19UCSC Ensembl
Innerchr7:42330330..42355599hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3825270
hg1925270
hg1825270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6340n100
Supporting Variantsnssv3752959
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)nsv1021700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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