A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654784



Internal ID18606379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10484627..10542865hg38UCSC Ensembl
Innerchr6:10484860..10543098hg19UCSC Ensembl
Innerchr6:10592846..10651084hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3858239
hg1958239
hg1858239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021023
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654784
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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