A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10571



Internal ID15195541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:102455440..102592617hg38UCSC Ensembl
Outerchr7:102095887..102233064hg19UCSC Ensembl
Outerchr7:101882892..102020133hg18UCSC Ensembl
Outerchr7:101689607..101826848hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38137178
hg19137178
hg18137242
hg17137242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879
Supporting Variants
SamplesNA18956
Known GenesALKBH4, LRWD1, MIR4467, MIR5090, ORAI2, POLR2J, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B
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)nssv10571
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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