A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700972



Internal ID15090938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162325327..162390870hg38UCSC Ensembl
Innerchr6:162746359..162811902hg19UCSC Ensembl
Innerchr6:162666349..162731892hg18UCSC Ensembl
Innerchr6:162716770..162782313hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3865544
hg1965544
hg1865544
hg1765544
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700972
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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