A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578623



Internal ID16019346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11930721..11934079hg38UCSC Ensembl
Innerchr19:12041536..12044894hg19UCSC Ensembl
Innerchr19:11902536..11905894hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383359
hg193359
hg183359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6269n54
Supporting Variantsnssv893561
Samples
Known GenesZNF700
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578623
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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