A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024620



Internal ID19113837
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 StatusM
Merged Variantsdgv6000n100
Supporting Variantsnssv3657663
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)nsv1024620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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