A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031450



Internal ID19120672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85918363..85953712hg38UCSC Ensembl
Innerchr7:85547679..85583028hg19UCSC Ensembl
Innerchr7:85385615..85420964hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3835350
hg1935350
hg1835350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655181
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)nsv1031450
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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