A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026268



Internal ID19115485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8630558..8658064hg38UCSC Ensembl
Innerchr7:8670188..8697694hg19UCSC Ensembl
Innerchr7:8636713..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 Variantsdgv6256n100
Supporting Variantsnssv3655128, nssv3655126, nssv3655129, nssv3655127, nssv3655132, nssv3655131, nssv3655130, nssv3655125
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)nsv1026268
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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