A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062596



Internal ID19151815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34825081..34887191hg38UCSC Ensembl
Innerchr19:35315985..35378095hg19UCSC Ensembl
Innerchr19:40007825..40069935hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3862111
hg1962111
hg1862111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3517n100
Supporting Variantsnssv3566597
Samples
Known GenesLOC400685
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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