A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997969



Internal ID19157506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625981..34638878hg38UCSC Ensembl
Innerchr1:35091582..35104479hg19UCSC Ensembl
Innerchr1:34864169..34877066hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812898
hg1912898
hg1812898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv146n100
Supporting Variantsnssv3465740
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997969
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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