A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10572



Internal ID15195540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102565462..102679356hg38UCSC Ensembl
Outerchr7:102205909..102319803hg19UCSC Ensembl
Outerchr7:101993015..102107039hg18UCSC Ensembl
Outerchr7:101799730..101913754hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38113895
hg19113895
hg18114025
hg17114025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879
Supporting Variants
SamplesNA18956
Known GenesPOLR2J2, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B, UPK3BL
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)nssv10572
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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