A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519863



Internal ID15447156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38278989..38377955hg38UCSC Ensembl
Innerchr7:38318590..38417556hg19UCSC Ensembl
Innerchr7:38285115..38384081hg18UCSC Ensembl
Innerchr7:38091830..38190796hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3898967
hg1998967
hg1898967
hg1798967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675803, nssv680494, nssv662520, nssv697651, nssv671558, nssv678359, nssv701002, nssv681291, nssv676287, nssv686988, nssv704497, nssv689834, nssv659151, nssv702948, nssv685970, nssv662519, nssv701170
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519863
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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