A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10987



Internal ID15192889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:8266731..8305858hg38UCSC Ensembl
Outerchr19:8331615..8370742hg19UCSC Ensembl
Outerchr19:8237615..8276742hg18UCSC Ensembl
Outerchr19:8237615..8276742hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839128
hg1939128
hg1839128
hg1739128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2401
Supporting Variants
SamplesNA15510
Known GenesCD320
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)nssv10987
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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