A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053624



Internal ID18796155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74437611..74487317hg38UCSC Ensembl
Innerchr10:76197369..76247075hg19UCSC Ensembl
Innerchr10:75867375..75917081hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3849707
hg1949707
hg1849707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv925n100
Supporting Variantsnssv3520076
Samples
Known GenesADK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053624
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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