A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv174



Internal ID15036971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36340817..36374513hg38UCSC Ensembl
Outerchr19:36831719..36865415hg19UCSC Ensembl
Outerchr19:41523559..41557255hg18UCSC Ensembl
Outerchr19:41523559..41557255hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3833697
hg1933697
hg1833697
hg1733697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv174
SamplesNA15510
Known GenesZFP14
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv174
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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