A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749027



Internal ID18700622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10466868..10535418hg38UCSC Ensembl
Innerchr6:10467101..10535651hg19UCSC Ensembl
Innerchr6:10575087..10643637hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3868551
hg1968551
hg1868551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029884
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)nssv3749027
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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