A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001492



Internal ID18744023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195094261..195214668hg38UCSC Ensembl
Innerchr3:194814990..194935397hg19UCSC Ensembl
Innerchr3:196296279..196416686hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38120408
hg19120408
hg18120408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611380
Samples
Known GenesXXYLT1, XXYLT1-AS1, XXYLT1-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001492
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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