A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605857



Internal ID16393266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2018299..2075768hg38UCSC Ensembl
Innerchr7:2057934..2115403hg19UCSC Ensembl
Innerchr7:2024460..2081929hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3857470
hg1957470
hg1857470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11143n54
Supporting Variantsnssv1155109
SamplesHGDP00433
Known GenesMAD1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605857
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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