A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021462



Internal ID19110679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38345240..38378564hg38UCSC Ensembl
Innerchr7:38384841..38418165hg19UCSC Ensembl
Innerchr7:38351366..38384690hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3833325
hg1933325
hg1833325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6336n100
Supporting Variantsnssv3643862, nssv3643861
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021462
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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