A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150144



Internal ID15854611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52562408..52611014hg38UCSC Ensembl
Innerchr19:53065661..53114267hg19UCSC Ensembl
Innerchr19:57757473..57806079hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3848607
hg1948607
hg1848607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580027
Supporting Variants
Samples1780862226_A
Known GenesZNF137P, ZNF701
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150144
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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