A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2528



Internal ID15200405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:50250334..50303239hg38UCSC Ensembl
Outerchr19:50753591..50806496hg19UCSC Ensembl
Outerchr19:55445403..55498308hg18UCSC Ensembl
Outerchr19:55445403..55498308hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3852906
hg1952906
hg1852906
hg1752906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9558
SamplesNA18507
Known GenesMYH14
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv2528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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