A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026521



Internal ID19115739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40143079..40180606hg38UCSC Ensembl
Innerchr7:40182678..40220205hg19UCSC Ensembl
Innerchr7:40149203..40186730hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3837528
hg1937528
hg1837528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6338n100
Supporting Variantsnssv3643874, nssv3643875
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)nsv1026521
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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