A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696915



Internal ID15433567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167037121..167060197hg38UCSC Ensembl
Innerchr6:167450609..167473685hg19UCSC Ensembl
Innerchr6:167370599..167393675hg18UCSC Ensembl
Innerchr6:167421020..167444096hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823077
hg1923077
hg1823077
hg1723077
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519550
Supporting Variants
Samples
Known GenesFGFR1OP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696915
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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