A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026022



Internal ID19115239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40400961..40439467hg38UCSC Ensembl
Innerchr7:40440560..40479066hg19UCSC Ensembl
Innerchr7:40407085..40445591hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3838507
hg1938507
hg1838507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6339n100
Supporting Variantsnssv3752953
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026022
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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