A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876102



Internal ID15823372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74428381..74627716hg38UCSC Ensembl
Innerchr17:72424520..72623855hg19UCSC Ensembl
Innerchr17:69936115..70135450hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38199336
hg19199336
hg18199336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576023
Supporting Variants
Samples
Known GenesC17orf77, CD300A, CD300C, CD300E, CD300LB, CD300LD, GPRC5C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876102
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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