A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028754



Internal ID19117972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76726803..76751356hg38UCSC Ensembl
Innerchr6:77436520..77461073hg19UCSC Ensembl
Innerchr6:77493239..77517792hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824554
hg1924554
hg1824554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3658873, nssv3658874, nssv3658872
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028754
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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