A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032400



Internal ID19121622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8631364..8658064hg38UCSC Ensembl
Innerchr7:8670994..8697694hg19UCSC Ensembl
Innerchr7:8637519..8664219hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3826701
hg1926701
hg1826701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6256n100
Supporting Variantsnssv3642746
Samples
Known GenesNXPH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032400
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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