A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701653



Internal ID15438305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169222622..169270846hg38UCSC Ensembl
Innerchr1:169191860..169240084hg19UCSC Ensembl
Innerchr1:167458484..167506708hg18UCSC Ensembl
Innerchr1:165923518..165971742hg17UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3848225
hg1948225
hg1848225
hg1748225
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525520
Supporting Variants
Samples
Known GenesNME7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701653
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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