A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2436



Internal ID15546999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19705049..19758362hg38UCSC Ensembl
Outerchr19:19815858..19869171hg19UCSC Ensembl
Outerchr19:19676858..19730171hg18UCSC Ensembl
Outerchr19:19676858..19730171hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3853314
hg1953314
hg1853314
hg1753314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6775, nssv5733, nssv2212
SamplesNA12156, NA18555, NA19129
Known GenesLINC00663, ZNF14
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)nsv2436
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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