A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038197



Internal ID19127416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69751325..69774427hg38UCSC Ensembl
Innerchr10:71511081..71534183hg19UCSC Ensembl
Innerchr10:71181087..71204189hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3823103
hg1923103
hg1823103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv921n100
Supporting Variantsnssv3522379, nssv3505397
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038197
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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