A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6256n100



Internal ID22792343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8630558..8658064hg38UCSC Ensembl
chr7:8670188..8697694hg19UCSC Ensembl
chr7:8636713..8664219hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3827507
hg1927507
hg1827507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033515, nsv1032400, nsv1026268
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)dgv6256n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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