A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028792



Internal ID19118010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142049538..142071110hg38UCSC Ensembl
Innerchr7:141749338..141770910hg19UCSC Ensembl
Innerchr7:141395807..141417379hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3821573
hg1921573
hg1821573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6646n100
Supporting Variantsnssv3664288
Samples
Known GenesMGAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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