A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657663



Internal ID18955944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65106986..65191027hg38UCSC Ensembl
Innerchr6:65816879..65900920hg19UCSC Ensembl
Innerchr6:65873600..65957641hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3884042
hg1984042
hg1884042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024620
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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