A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10201



Internal ID15542597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:112143297..112172176hg38UCSC Ensembl
Outerchr1:112685919..112714798hg19UCSC Ensembl
Outerchr1:112487442..112516321hg18UCSC Ensembl
Outerchr1:112397961..112426840hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3828880
hg1928880
hg1828880
hg1728880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2443
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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