A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021023



Internal ID18763557
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 StatusM
Merged Variantsdgv5918n100
Supporting Variantsnssv3654784
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)nsv1021023
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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